Variant report

Variant	nsv907709
Chromosome Location	chr17:15851196-15937487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2918)
CpG islands
(count:1529)
Chromatin interactive
region (count:114)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:2918 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:15902968-15903142	K562	blood:	n/a	n/a
2	ARID3A	chr17:15862124-15862878	K562	blood:	n/a	n/a
3	ARID3A	chr17:15931068-15932170	K562	blood:	n/a	n/a
4	ARID3A	chr17:15901834-15902081	HepG2	liver:	n/a	n/a
5	ARID3A	chr17:15901668-15902127	K562	blood:	n/a	n/a
6	ARID3A	chr17:15914877-15915353	HepG2	liver:	n/a	n/a
7	ARID3A	chr17:15902481-15903240	HepG2	liver:	n/a	n/a
8	ARID3A	chr17:15862592-15862696	HepG2	liver:	n/a	n/a
9	ARID3A	chr17:15869288-15870075	HepG2	liver:	n/a	n/a
10	ARID3A	chr17:15885154-15885723	K562	blood:	n/a	n/a
11	ARID3A	chr17:15929429-15929620	K562	blood:	n/a	n/a
12	ARID3A	chr17:15917080-15917553	HepG2	liver:	n/a	n/a
13	ATF1	chr17:15930958-15931807	K562	blood:	n/a	n/a
14	ATF1	chr17:15885244-15885573	K562	blood:	n/a	n/a
15	ATF1	chr17:15862062-15862804	K562	blood:	n/a	n/a
16	ATF1	chr17:15875851-15876087	K562	blood:	n/a	n/a
17	ATF1	chr17:15902769-15903231	K562	blood:	n/a	n/a
18	ATF2	chr17:15884411-15884928	GM12878	blood:	n/a	n/a
19	ATF2	chr17:15902715-15903257	GM12878	blood:	n/a	n/a
20	ATF2	chr17:15931264-15931818	GM12878	blood:	n/a	n/a
21	ATF2	chr17:15869409-15870334	H1-hESC	embryonic stem cell:	n/a	chr17:15869886-15869893
22	ATF2	chr17:15902507-15903189	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF2	chr17:15884539-15884890	GM12878	blood:	n/a	n/a
24	ATF2	chr17:15869467-15870240	H1-hESC	embryonic stem cell:	n/a	chr17:15869886-15869893
25	ATF2	chr17:15930985-15931892	GM12878	blood:	n/a	n/a
26	ATF2	chr17:15862096-15862864	GM12878	blood:	n/a	n/a
27	ATF2	chr17:15902636-15903255	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr17:15862152-15862876	GM12878	blood:	n/a	n/a
29	ATF3	chr17:15902763-15903342	A549	lung:	n/a	chr17:15902790-15902799
30	ATF3	chr17:15862158-15862877	K562	blood:	n/a	n/a
31	ATF3	chr17:15902730-15903281	A549	lung:	n/a	chr17:15902790-15902799
32	ATF3	chr17:15902819-15903127	K562	blood:	n/a	n/a
33	ATF3	chr17:15855382-15855528	K562	blood:	n/a	n/a
34	ATF3	chr17:15862405-15862898	HCT-116	colon:	n/a	n/a
35	ATF3	chr17:15862386-15862953	HCT-116	colon:	n/a	n/a
36	ATF3	chr17:15931346-15931800	K562	blood:	n/a	n/a
37	BACH1	chr17:15902645-15903078	H1-hESC	embryonic stem cell:	n/a	n/a
38	BACH1	chr17:15869603-15870225	H1-hESC	embryonic stem cell:	n/a	n/a
39	BACH1	chr17:15885175-15885548	K562	blood:	n/a	chr17:15885331-15885345
40	BACH1	chr17:15885110-15885621	H1-hESC	embryonic stem cell:	n/a	chr17:15885331-15885345
41	BACH1	chr17:15862180-15862785	K562	blood:	n/a	chr17:15862644-15862658
42	BACH1	chr17:15853305-15853413	K562	blood:	n/a	n/a
43	BACH1	chr17:15924260-15924267	K562	blood:	n/a	n/a
44	BATF	chr17:15884479-15884852	GM12878	blood:	n/a	n/a
45	BATF	chr17:15862332-15862867	GM12878	blood:	n/a	chr17:15862612-15862622
46	BATF	chr17:15860556-15860807	GM12878	blood:	n/a	chr17:15860698-15860708 chr17:15860697-15860708
47	BATF	chr17:15931441-15931778	GM12878	blood:	n/a	chr17:15931582-15931593 chr17:15931624-15931635
48	BATF	chr17:15931410-15931855	GM12878	blood:	n/a	chr17:15931582-15931593 chr17:15931624-15931635
49	BATF	chr17:15904612-15904828	GM12878	blood:	n/a	chr17:15904756-15904767 chr17:15904700-15904711 chr17:15904723-15904734
50	BATF	chr17:15862092-15862942	GM12878	blood:	n/a	chr17:15862612-15862622

(count:1529 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15878667-15878717	GM12892	blood:	n/a
2	chr17:15903687-15903737	PrEC	prostate:	n/a
3	chr17:15902694-15902744	AG10803	skin:	n/a
4	chr17:15902541-15902591	HAEpiC	amniotic membrane:	n/a
5	chr17:15878667-15878717	GM12892	blood:	n/a
6	chr17:15903687-15903737	PrEC	prostate:	n/a
7	chr17:15902694-15902744	AG10803	skin:	n/a
8	chr17:15902541-15902591	HAEpiC	amniotic membrane:	n/a
9	chr17:15903687-15903737	AG04450	lung:	fetal
10	chr17:15902560-15902610	SK-N-SH	brain:	n/a
11	chr17:15880379-15880429	HCT-116	colon:	n/a
12	chr17:15902795-15902845	HCPEpiC	choroid plexus:	n/a
13	chr17:15902694-15902744	AoSMC	blood vessel:	n/a
14	chr17:15902660-15902710	PFSK-1	brain:	n/a
15	chr17:15903096-15903146	GM19239	blood:	n/a
16	chr17:15902837-15902887	NHDF-neo	bronchial:	n/a
17	chr17:15902837-15902887	Hepatocyte	liver:	n/a
18	chr17:15902795-15902845	SK-N-SH_RA	brain:	n/a
19	chr17:15903096-15903146	GM12891	blood:	n/a
20	chr17:15869607-15869657	RPTEC	kidney:	n/a
21	chr17:15878667-15878717	BJ	skin:	n/a
22	chr17:15902795-15902845	AG09319	gingival:	n/a
23	chr17:15902560-15902610	GM06990	blood:	n/a
24	chr17:15880379-15880429	HepG2	liver:	n/a
25	chr17:15902952-15903002	LNCaP	prostate:	n/a
26	chr17:15902660-15902710	ECC-1	luminal epithelium:	n/a
27	chr17:15885326-15885376	PFSK-1	brain:	n/a
28	chr17:15903290-15903340	GM12891	blood:	n/a
29	chr17:15903290-15903340	HMEC	breast:	n/a
30	chr17:15880379-15880429	IMR90	lung:	fetal
31	chr17:15903687-15903737	K562	blood:	n/a
32	chr17:15853470-15853520	AoSMC	blood vessel:	n/a
33	chr17:15885326-15885376	PrEC	prostate:	n/a
34	chr17:15931082-15931132	T-47D	breast:	n/a
35	chr17:15902952-15903002	AG09309	skin:	n/a
36	chr17:15902694-15902744	HUVEC	blood vessel:	n/a
37	chr17:15902633-15902683	HCF	heart:	n/a
38	chr17:15901788-15901838	NB4	blood:	n/a
39	chr17:15902560-15902610	NT2-D1	testis:	n/a
40	chr17:15917660-15917710	HMEC	breast:	n/a
41	chr17:15902952-15903002	Jurkat	blood:	n/a
42	chr17:15899410-15899460	A549	lung:	n/a
43	chr17:15902952-15903002	HCM	heart:	n/a
44	chr17:15917660-15917710	AG09319	gingival:	n/a
45	chr17:15903096-15903146	LNCaP	prostate:	n/a
46	chr17:15902837-15902887	HCM	heart:	n/a
47	chr17:15903096-15903146	NH-A	brain:	n/a
48	chr17:15902952-15903002	PFSK-1	brain:	n/a
49	chr17:15901788-15901838	H1-hESC	embryonic stem cell:	embryo
50	chr17:15878667-15878717	HRPEpiC	eye:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr17:15903246..15906052-chr17:15922157..15923827,2	K562	blood:
2	chr17:15920209..15922955-chr17:15924177..15926730,2	K562	blood:
3	chr17:15902512..15905942-chr17:15916093..15919124,5	K562	blood:
4	chr17:15866407..15869569-chr17:15884863..15887251,3	K562	blood:
5	chr17:15902947..15903675-chr3:13036144..13036734,2	HCT-116	colon:
6	chr17:15850283..15852272-chr17:15862525..15865065,2	K562	blood:
7	chr17:15920209..15922955-chr17:15924177..15926730,2	K562	blood:
8	chr17:15874041..15877357-chr17:15878347..15881339,3	K562	blood:
9	chr17:15917993..15922048-chr17:15928334..15931723,4	MCF-7	breast:
10	chr17:15860952..15862454-chr17:15899696..15901427,2	K562	blood:
11	chr17:15905164..15907778-chr17:15930822..15933599,2	K562	blood:
12	chr17:15553526..15556124-chr17:15902249..15904435,2	MCF-7	breast:
13	chr17:15848087..15850037-chr17:15852392..15854859,2	K562	blood:
14	chr17:15901579..15902443-chr17:74732789..74733488,2	NB4	blood:
15	chr17:15860784..15862668-chr17:15867479..15869134,2	MCF-7	breast:
16	chr17:15864704..15867341-chr17:15873793..15875461,2	K562	blood:
17	chr17:15864704..15867341-chr17:15873793..15875461,2	K562	blood:
18	chr17:15926454..15928435-chr17:15932440..15934895,2	MCF-7	breast:
19	chr17:15902768..15903899-chr17:28443566..28444410,4	Hela-S3	cervix:
20	chr17:15903168..15903881-chr5:20690072..20690742,2	Hela-S3	cervix:
21	chr17:15860784..15862668-chr17:15867479..15869134,2	MCF-7	breast:
22	chr17:15848046..15849969-chr17:15901406..15903295,2	MCF-7	breast:
23	chr17:15903003..15903658-chr3:58419013..58419568,2	Hela-S3	cervix:
24	chr17:15903242..15905259-chr17:15927209..15928896,2	K562	blood:
25	chr17:15905982..15907631-chr17:15908656..15910993,3	K562	blood:
26	chr17:15852422..15855230-chr17:15859382..15862010,2	MCF-7	breast:
27	chr17:15907457..15909549-chr17:15927194..15929439,2	MCF-7	breast:
28	chr17:15884378..15885886-chr17:15892555..15894093,2	K562	blood:
29	chr11:125439057..125439579-chr17:15902732..15903484,2	NB4	blood:
30	chr17:15902503..15903133-chr2:47403392..47404131,2	Hela-S3	cervix:
31	chr17:15902291..15902878-chr2:128284164..128285109,2	Hela-S3	cervix:
32	chr17:15905164..15907778-chr17:15930822..15933599,2	K562	blood:
33	chr17:15924357..15928221-chr17:15933368..15936168,3	K562	blood:
34	chr17:15847910..15848845-chr17:15901471..15902383,2	MCF-7	breast:
35	chr1:201979391..201980146-chr17:15902285..15903134,2	HCT-116	colon:
36	chr17:15935922..15937736-chr17:15946128..15948484,2	K562	blood:
37	chr17:15884386..15887034-chr17:15891736..15894055,2	K562	blood:
38	chr17:15902634..15904373-chr17:15919410..15923219,3	MCF-7	breast:
39	chr17:15869541..15871982-chr17:15871991..15874515,2	K562	blood:
40	chr17:15925841..15927896-chr17:15930022..15931528,2	K562	blood:
41	chr17:15910738..15912780-chr17:15917922..15919655,2	K562	blood:
42	chr17:15901865..15904758-chr17:15916069..15919403,5	MCF-7	breast:
43	chr17:15902723..15903444-chr6:33239440..33240262,2	Hela-S3	cervix:
44	chr17:15918728..15924279-chr17:15927914..15931403,6	K562	blood:
45	chr17:15866407..15869569-chr17:15884863..15887251,3	K562	blood:
46	chr17:15869541..15871982-chr17:15871991..15874515,2	K562	blood:
47	chr17:15846803..15850519-chr17:15901644..15904167,3	MCF-7	breast:
48	chr17:15861872..15864251-chr17:15873905..15876165,2	K562	blood:
49	chr17:15861872..15863395-chr17:15873905..15875556,2	K562	blood:
50	chr17:15850283..15852272-chr17:15862525..15865065,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADORA2B-1	chr17:15884512-15885318	predAs_engstrom06_BC031588_1
2	lnc-ZSWIM7-2	chr17:15883557-15883681	NONHSAT145880
3	lnc-ZSWIM7-2	chr17:15880893-15881227	NONHSAT145880
4	lnc-ZSWIM7-2	chr17:15879883-15880406	NONHSAT145880
5	lnc-ZSWIM7-2	chr17:15881358-15881477	NONHSAT145880

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	NCOR1	hsa-let-7b-5p	chr17:15934835-15934829
2	TTC19	hsa-miR-30c-5p	chr17:15930416-15930438
3	ADORA2B	hsa-miR-27b-3p	chr17:15878973-15878980
4	ADORA2B	hsa-miR-27b-3p	chr17:15878960-15878980

Variant related genes	Relation type
ADORA2B	TF binding region
TTC19	TF binding region
ZSWIM7	TF binding region
ADORA2B	CpG island
TTC19	CpG island
ZSWIM7	CpG island
ENSG00000126653	chromatin interactions
ENSG00000144895	chromatin interactions
ENSG00000108474	chromatin interactions
ENSG00000141027	chromatin interactions
ENSG00000214941	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000144711	chromatin interactions
ENSG00000170425	chromatin interactions
ENSG00000168291	chromatin interactions
ENSG00000227790	chromatin interactions
ENSG00000251192	chromatin interactions
ENSG00000120742	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000161547	chromatin interactions
ENSG00000143933	chromatin interactions
ENSG00000011295	chromatin interactions
ENSG00000230844	chromatin interactions
ENSG00000092931	chromatin interactions
ENSG00000149547	chromatin interactions
ENSG00000199071	chromatin interactions
ENSG00000251537	chromatin interactions
ENSG00000163166	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000231500	chromatin interactions
ENSG00000266261	chromatin interactions
ENSG00000075413	chromatin interactions
ENSG00000243686	chromatin interactions

Extended variants
information (count: 3541 )
Associated
traits (count: 171 )

Variant overlapped rSNPs/rCNVs (count:3541 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs758856	chr17:15851196-15851197	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs548065124	chr17:15851221-15851222	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs541434091	chr17:15851259-15851260	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs561742646	chr17:15851293-15851294	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs567863717	chr17:15851387-15851388	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs527578049	chr17:15851429-15851430	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs187110486	chr17:15851471-15851472	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs550124696	chr17:15851494-15851495	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs373469110	chr17:15851498-15851499	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs56339443	chr17:15851512-15851513	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs374330573	chr17:15851517-15851518	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs7208072	chr17:15851559-15851560	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558661359	chr17:15851578-15851579	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs373739153	chr17:15851593-15851594	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs565727537	chr17:15851610-15851611	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs201898050	chr17:15851620-15851621	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs150453210	chr17:15851621-15851622	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs566072443	chr17:15851622-15851623	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
19	rs56317334	chr17:15851623-15851624	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
20	rs199931070	chr17:15851625-15851626	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
21	rs534756547	chr17:15851637-15851638	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs76392987	chr17:15851655-15851656	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs573868117	chr17:15851667-15851668	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
24	rs542777223	chr17:15851698-15851699	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs7208108	chr17:15851706-15851707	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs61613212	chr17:15851714-15851715	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs2779198	chr17:15851715-15851716	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
28	rs9901942	chr17:15851717-15851718	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
29	rs111619042	chr17:15851718-15851719	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
30	rs56222691	chr17:15851721-15851722	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
31	rs545112363	chr17:15851744-15851745	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
32	rs192666546	chr17:15851755-15851756	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
33	rs527236974	chr17:15851763-15851764	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
34	rs184412223	chr17:15851783-15851784	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
35	rs142680549	chr17:15851784-15851785	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
36	rs549567136	chr17:15851797-15851798	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs530352335	chr17:15851798-15851799	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs367574302	chr17:15851801-15851802	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs190526783	chr17:15851814-15851815	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs528883830	chr17:15851817-15851818	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs550480832	chr17:15851879-15851880	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs569899881	chr17:15851899-15851900	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs757623	chr17:15851921-15851922	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs117360362	chr17:15852031-15852032	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs193101951	chr17:15852039-15852040	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs76930117	chr17:15852041-15852042	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs550631763	chr17:15852047-15852048	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs140691561	chr17:15852058-15852059	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs185125923	chr17:15852061-15852062	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs568469981	chr17:15852070-15852071	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:171)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3550 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15849000-15852000	Enhancers	Spleen	Spleen
2	chr17:15849400-15851200	Enhancers	Gastric	stomach
3	chr17:15849400-15851400	Bivalent Enhancer	Fetal Stomach	stomach
4	chr17:15849400-15852200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
5	chr17:15849600-15851800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr17:15849600-15852000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr17:15849600-15852000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr17:15849600-15852200	Enhancers	Stomach Mucosa	stomach
9	chr17:15849600-15860600	Weak transcription	Pancreas	Pancrea
10	chr17:15849800-15851200	Enhancers	Colon Smooth Muscle	Colon
11	chr17:15849800-15851200	Weak transcription	Right Atrium	heart
12	chr17:15849800-15851400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr17:15849800-15851600	Flanking Active TSS	HepG2	liver
14	chr17:15849800-15852000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
15	chr17:15849800-15852000	Active TSS	Rectal Smooth Muscle	rectum
16	chr17:15849800-15852200	Enhancers	Placenta	Placenta
17	chr17:15849800-15852200	Enhancers	Sigmoid Colon	Sigmoid Colon
18	chr17:15850000-15851400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr17:15850000-15851400	Enhancers	HSMM	muscle
20	chr17:15850000-15851600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr17:15850000-15851600	Flanking Active TSS	Colonic Mucosa	Colon
22	chr17:15850000-15852200	Enhancers	Fetal Intestine Large	intestine
23	chr17:15850000-15852200	Enhancers	Hela-S3	cervix
24	chr17:15850000-15852200	Flanking Active TSS	HMEC	breast
25	chr17:15850200-15851200	Weak transcription	Left Ventricle	heart
26	chr17:15850200-15851400	Enhancers	HSMMtube	muscle
27	chr17:15850200-15851600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
28	chr17:15850200-15851600	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
29	chr17:15850200-15852200	Enhancers	Esophagus	oesophagus
30	chr17:15850200-15854600	Weak transcription	Right Ventricle	heart
31	chr17:15850200-15859200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr17:15850200-15860600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr17:15850400-15851200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr17:15850400-15851400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr17:15850400-15851600	Enhancers	Fetal Muscle Leg	muscle
36	chr17:15850400-15852200	Enhancers	Placenta Amnion	Placenta Amnion
37	chr17:15850400-15856600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr17:15850600-15851200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr17:15850600-15851200	Enhancers	HUVEC	blood vessel
40	chr17:15850600-15851400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr17:15850600-15851600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr17:15850600-15851600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr17:15850600-15851600	Enhancers	Fetal Intestine Small	intestine
44	chr17:15850600-15852000	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr17:15850800-15851200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr17:15850800-15851200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr17:15850800-15851200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr17:15850800-15851200	Enhancers	NHDF-Ad	bronchial
49	chr17:15850800-15851200	Enhancers	NHLF	lung
50	chr17:15850800-15851400	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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