Variant report

Variant	nsv887766
Chromosome Location	chr7:16883936-16991565
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1411)
CpG islands
(count:1220)
Chromatin interactive
region (count:101)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1411 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:16967623-16968007	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:16954335-16954897	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:16886912-16887247	HepG2	liver:	n/a	n/a
4	ATF1	chr7:16955835-16955974	K562	blood:	n/a	n/a
5	ATF1	chr7:16920513-16920521	K562	blood:	n/a	n/a
6	ATF1	chr7:16938123-16938126	K562	blood:	n/a	n/a
7	ATF3	chr7:16955783-16956099	K562	blood:	n/a	n/a
8	ATF3	chr7:16886770-16887562	A549	lung:	n/a	n/a
9	ATF3	chr7:16944740-16945401	A549	lung:	n/a	n/a
10	ATF3	chr7:16886801-16887449	A549	lung:	n/a	n/a
11	BCL3	chr7:16886626-16887591	A549	lung:	n/a	n/a
12	BCL3	chr7:16944766-16945589	A549	lung:	n/a	n/a
13	BCL3	chr7:16944794-16945427	A549	lung:	n/a	n/a
14	BCL3	chr7:16886665-16887601	A549	lung:	n/a	n/a
15	BHLHE40	chr7:16955793-16956042	K562	blood:	n/a	n/a
16	BRCA1	chr7:16955847-16956041	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr7:16886387-16887480	Hela-S3	cervix:	n/a	chr7:16886665-16886672
18	CBX3	chr7:16987785-16987980	K562	blood:	n/a	n/a
19	CEBPB	chr7:16939841-16940183	HepG2	liver:	n/a	chr7:16940012-16940023
20	CEBPB	chr7:16954446-16954746	MCF-7	breast:	n/a	chr7:16954714-16954722
21	CEBPB	chr7:16954431-16954728	A549	lung:	n/a	chr7:16954714-16954722
22	CEBPB	chr7:16954416-16954663	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:16954349-16954765	HepG2	liver:	n/a	chr7:16954714-16954722
24	CEBPB	chr7:16961496-16962032	MCF-7	breast:	n/a	n/a
25	CEBPB	chr7:16954913-16955512	MCF-7	breast:	n/a	chr7:16955093-16955110
26	CEBPB	chr7:16886925-16887186	IMR90	lung:	n/a	chr7:16887030-16887041
27	CEBPB	chr7:16903709-16903939	HepG2	liver:	n/a	n/a
28	CEBPB	chr7:16991314-16991533	IMR90	lung:	n/a	n/a
29	CEBPB	chr7:16886843-16887410	A549	lung:	n/a	chr7:16887030-16887041
30	CEBPB	chr7:16955021-16955446	IMR90	lung:	n/a	chr7:16955093-16955110
31	CEBPB	chr7:16886822-16887457	A549	lung:	n/a	chr7:16887030-16887041
32	CEBPB	chr7:16895239-16895386	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr7:16961490-16961858	MCF-7	breast:	n/a	n/a
34	CEBPB	chr7:16948444-16948631	IMR90	lung:	n/a	n/a
35	CEBPB	chr7:16895188-16895415	IMR90	lung:	n/a	n/a
36	CEBPB	chr7:16939841-16940168	IMR90	lung:	n/a	chr7:16940012-16940023
37	CEBPB	chr7:16954357-16954771	HepG2	liver:	n/a	chr7:16954714-16954722
38	CEBPB	chr7:16966632-16967029	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr7:16939825-16940248	MCF-7	breast:	n/a	chr7:16940012-16940023
40	CEBPB	chr7:16934284-16934399	A549	lung:	n/a	n/a
41	CEBPB	chr7:16886263-16887556	MCF-7	breast:	n/a	chr7:16887030-16887041
42	CEBPB	chr7:16955799-16956080	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr7:16955017-16955459	MCF-7	breast:	n/a	chr7:16955093-16955110
44	CEBPB	chr7:16886566-16887551	A549	lung:	n/a	chr7:16887030-16887041
45	CEBPB	chr7:16886171-16887513	MCF-7	breast:	n/a	chr7:16887030-16887041
46	CEBPB	chr7:16939849-16940196	A549	lung:	n/a	chr7:16940012-16940023
47	CEBPB	chr7:16954380-16954637	HepG2	liver:	n/a	n/a
48	CEBPB	chr7:16975016-16975338	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr7:16886195-16887591	Hela-S3	cervix:	n/a	chr7:16887030-16887041
50	CEBPB	chr7:16939900-16940158	Hela-S3	cervix:	n/a	chr7:16940012-16940023

(count:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:16893769-16893819	IMR90	lung:	fetal
2	chr7:16913845-16913895	GM06990	blood:	n/a
3	chr7:16890769-16890819	Caco-2	colon:	n/a
4	chr7:16922421-16922471	HEK293	kidney:	embryo
5	chr7:16966323-16966373	GM12892	blood:	n/a
6	chr7:16921699-16921749	Hepatocyte	liver:	n/a
7	chr7:16922326-16922376	PANC-1	pancreas:	n/a
8	chr7:16921699-16921749	MCF10A-Er-Src	breast:	n/a
9	chr7:16892988-16893038	HCF	heart:	n/a
10	chr7:16945442-16945492	HEK293	kidney:	embryo
11	chr7:16890431-16890481	GM12891	blood:	n/a
12	chr7:16892988-16893038	LNCaP	prostate:	n/a
13	chr7:16913845-16913895	NT2-D1	testis:	n/a
14	chr7:16966323-16966373	NB4	blood:	n/a
15	chr7:16893769-16893819	RPTEC	kidney:	n/a
16	chr7:16890769-16890819	LNCaP	prostate:	n/a
17	chr7:16922421-16922471	PrEC	prostate:	n/a
18	chr7:16890879-16890929	HL-60	blood:	n/a
19	chr7:16890973-16891023	AG09309	skin:	n/a
20	chr7:16920271-16920321	ProgFib	skin:	n/a
21	chr7:16945442-16945492	HRCEpiC	kidney:	n/a
22	chr7:16966323-16966373	A549	lung:	n/a
23	chr7:16945442-16945492	ECC-1	luminal epithelium:	n/a
24	chr7:16921699-16921749	HepG2	liver:	n/a
25	chr7:16921699-16921749	ECC-1	luminal epithelium:	n/a
26	chr7:16922421-16922471	HPAEpiC	pulmonary alveolar:	n/a
27	chr7:16887412-16887462	AG04450	lung:	fetal
28	chr7:16913845-16913895	A549	lung:	n/a
29	chr7:16966323-16966373	HPAEpiC	pulmonary alveolar:	n/a
30	chr7:16921699-16921749	AG04450	lung:	fetal
31	chr7:16922492-16922542	AG04449	skin:	fetal
32	chr7:16922421-16922471	HCPEpiC	choroid plexus:	n/a
33	chr7:16890879-16890929	BJ	skin:	n/a
34	chr7:16893769-16893819	HRCEpiC	kidney:	n/a
35	chr7:16891079-16891129	GM12878	blood:	n/a
36	chr7:16891079-16891129	HRPEpiC	eye:	n/a
37	chr7:16922421-16922471	PANC-1	pancreas:	n/a
38	chr7:16913845-16913895	AG09319	gingival:	n/a
39	chr7:16890769-16890819	AG04449	skin:	fetal
40	chr7:16890769-16890819	HEEpiC	esophagus:	n/a
41	chr7:16956550-16956600	H1-hESC	embryonic stem cell:	embryo
42	chr7:16920271-16920321	HCT-116	colon:	n/a
43	chr7:16955875-16955925	CMK	blood:	n/a
44	chr7:16922326-16922376	HRPEpiC	eye:	n/a
45	chr7:16913845-16913895	HUVEC	blood vessel:	n/a
46	chr7:16887412-16887462	HUVEC	blood vessel:	n/a
47	chr7:16956550-16956600	GM06990	blood:	n/a
48	chr7:16913845-16913895	GM12878	blood:	n/a
49	chr7:16913845-16913895	BE2_C	brain:	n/a
50	chr7:16890775-16890825	K562	blood:	n/a

(count:101 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:16840761..16845436-chr7:16917964..16923686,10	MCF-7	breast:
2	chr7:16842180..16845555-chr7:16959624..16963006,3	MCF-7	breast:
3	chr7:16843687..16847356-chr7:16880969..16885089,4	MCF-7	breast:
4	chr7:16973521..16976963-chr7:16980270..16983523,4	MCF-7	breast:
5	chr7:16960280..16962673-chr7:16969030..16970953,2	MCF-7	breast:
6	chr7:16842139..16846678-chr7:16885089..16889372,16	MCF-7	breast:
7	chr7:16847748..16852819-chr7:16884544..16888713,8	MCF-7	breast:
8	chr7:16930305..16931804-chr7:16957626..16958588,7	MCF-7	breast:
9	chr7:16852860..16855364-chr7:16884704..16887275,2	MCF-7	breast:
10	chr7:16944622..16945221-chr7:16961355..16961992,2	MCF-7	breast:
11	chr7:16974533..16976554-chr7:17579096..17580960,2	K562	blood:
12	chr7:16884365..16886656-chr7:16921143..16924062,2	MCF-7	breast:
13	chr7:16795433..16797720-chr7:16943125..16945595,2	MCF-7	breast:
14	chr7:16892686..16894527-chr7:16894873..16896897,2	MCF-7	breast:
15	chr7:16966075..16967859-chr7:16969900..16971992,2	MCF-7	breast:
16	chr7:16886651..16887248-chr7:16961321..16961836,2	MCF-7	breast:
17	chr7:16882638..16888125-chr7:16917806..16922749,7	MCF-7	breast:
18	chr7:16962681..16964346-chr7:16965183..16967414,2	MCF-7	breast:
19	chr7:16735209..16736046-chr7:16956706..16957580,3	K562	blood:
20	chr7:16885940..16887633-chr7:16888107..16889643,2	MCF-7	breast:
21	chr7:16966017..16967722-chr7:16978514..16980998,2	MCF-7	breast:
22	chr7:16954984..16957560-chr7:16961614..16963759,2	MCF-7	breast:
23	chr7:16793190..16795518-chr7:16923523..16926249,2	MCF-7	breast:
24	chr7:16825159..16826158-chr7:16919904..16920435,2	MCF-7	breast:
25	chr7:16886651..16887248-chr7:16961321..16961836,2	MCF-7	breast:
26	chr7:16973925..16976162-chr7:16977721..16980003,2	K562	blood:
27	chr7:16876778..16878697-chr7:16884099..16885965,2	MCF-7	breast:
28	chr7:16973521..16976963-chr7:16980270..16983523,4	MCF-7	breast:
29	chr7:16885425..16887633-chr7:16956037..16959031,2	MCF-7	breast:
30	chr7:16944903..16947549-chr7:16951008..16952763,2	MCF-7	breast:
31	chr7:16957723..16959787-chr7:16960237..16962580,2	K562	blood:
32	chr7:16885940..16887633-chr7:16888107..16889643,2	MCF-7	breast:
33	chr7:16942340..16948340-chr7:16954410..16958338,5	MCF-7	breast:
34	chr7:16920618..16921311-chr8:99380929..99381723,2	MCF-7	breast:
35	chr7:16960280..16962673-chr7:16969030..16970953,2	MCF-7	breast:
36	chr7:16956640..16958922-chr7:17019855..17022543,2	MCF-7	breast:
37	chr7:16944622..16945221-chr7:16961355..16961992,2	MCF-7	breast:
38	chr7:16930864..16931608-chr7:16957731..16958689,3	MCF-7	breast:
39	chr7:16973110..16976162-chr7:16977705..16980003,3	K562	blood:
40	chr7:16942340..16948340-chr7:16954410..16958338,5	MCF-7	breast:
41	chr7:16878823..16881693-chr7:16881989..16884135,2	K562	blood:
42	chr7:16885425..16887633-chr7:16956037..16959031,2	MCF-7	breast:
43	chr7:16929331..16931159-chr7:16956087..16958854,2	MCF-7	breast:
44	chr7:16962023..16963912-chr7:16979161..16982109,2	K562	blood:
45	chr7:16843341..16846175-chr7:16955104..16957919,2	MCF-7	breast:
46	chr7:16839543..16841251-chr7:16918984..16920555,2	MCF-7	breast:
47	chr7:16961828..16963481-chr7:16965140..16966973,2	K562	blood:
48	chr7:16882221..16884477-chr7:16885403..16887201,3	MCF-7	breast:
49	chr7:16930587..16933448-chr7:16954480..16956101,2	MCF-7	breast:
50	chr7:16930305..16931804-chr7:16957626..16958588,7	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AGR2-1	chr7:16921568-16921597	NONHSAT119307
2	lnc-TSPAN13-1	chr7:16928245-16928509	NONHSAT119308
3	lnc-AGR2-1	chr7:16913040-16913467	NONHSAT119307
4	lnc-TSPAN13-2	chr7:16977849-16978181	NONHSAT119309
5	lnc-AGR2-1	chr7:16918134-16918269	NONHSAT119307

No data

Variant related genes	Relation type
ENSG00000227965	TF binding region
RAD17P1	TF binding region
ENSG00000270593	TF binding region
AGR3	TF binding region
ENSG00000223867	TF binding region
ENSG00000227965	CpG island
RAD17P1	CpG island
ENSG00000270593	CpG island
AGR3	CpG island
ENSG00000223867	CpG island
ENSG00000237773	chromatin interactions
ENSG00000106541	chromatin interactions
ENSG00000223867	chromatin interactions
ENSG00000232400	chromatin interactions
ENSG00000229688	chromatin interactions
ENSG00000173467	chromatin interactions
ENSG00000227965	chromatin interactions
ENSG00000228675	chromatin interactions
ENSG00000106546	chromatin interactions

Extended variants
information (count: 5062 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:5062 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12668575	chr7:16883936-16883937	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573007807	chr7:16883950-16883951	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs373901187	chr7:16883965-16883966	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs577692845	chr7:16883989-16883990	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs189248547	chr7:16883990-16883991	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs558915698	chr7:16883997-16883998	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs151113236	chr7:16884003-16884004	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs191898310	chr7:16884017-16884018	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182994428	chr7:16884019-16884020	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs565185905	chr7:16884027-16884028	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs187505787	chr7:16884040-16884041	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs371546819	chr7:16884041-16884042	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs575604192	chr7:16884090-16884091	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs550271117	chr7:16884097-16884098	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367705453	chr7:16884111-16884112	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs75014006	chr7:16884124-16884125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs141074505	chr7:16884141-16884142	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs57496705	chr7:16884145-16884146	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs557481934	chr7:16884187-16884188	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs150303640	chr7:16884204-16884205	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs566891865	chr7:16884209-16884210	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs35170620	chr7:16884221-16884222	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs17136737	chr7:16884241-16884242	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs555772701	chr7:16884268-16884269	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs577652993	chr7:16884297-16884298	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs191690180	chr7:16884299-16884300	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs545133873	chr7:16884305-16884306	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs571113176	chr7:16884307-16884308	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs183833820	chr7:16884309-16884310	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs12672876	chr7:16884311-16884312	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs572999842	chr7:16884320-16884321	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs137872432	chr7:16884337-16884338	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs532072261	chr7:16884366-16884367	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs546696196	chr7:16884414-16884415	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543824827	chr7:16884423-16884424	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs565322000	chr7:16884478-16884479	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs142102824	chr7:16884479-16884480	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs559952429	chr7:16884519-16884520	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs532744387	chr7:16884547-16884548	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs566510002	chr7:16884581-16884582	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs186961900	chr7:16884599-16884600	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs552492851	chr7:16884637-16884638	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs561447547	chr7:16884655-16884656	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs548790567	chr7:16884657-16884658	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs368181674	chr7:16884658-16884659	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs538988556	chr7:16884663-16884664	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs567205692	chr7:16884664-16884665	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs201516079	chr7:16884665-16884666	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs547349795	chr7:16884698-16884699	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs192273825	chr7:16884722-16884723	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495309	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16880000-16886200	Weak transcription	Placenta	Placenta
2	chr7:16880400-16889600	Weak transcription	Gastric	stomach
3	chr7:16881800-16886400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:16881800-16887000	Weak transcription	Osteobl	bone
5	chr7:16882600-16885000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr7:16885000-16885200	Enhancers	Placenta Amnion	Placenta Amnion
7	chr7:16885200-16885600	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr7:16885200-16885800	Enhancers	A549	lung
9	chr7:16885200-16886800	Enhancers	Fetal Intestine Large	intestine
10	chr7:16885200-16886800	Enhancers	Fetal Intestine Small	intestine
11	chr7:16885600-16886000	Enhancers	Placenta Amnion	Placenta Amnion
12	chr7:16885600-16886200	Enhancers	Hela-S3	cervix
13	chr7:16885800-16886000	Enhancers	Fetal Kidney	kidney
14	chr7:16885800-16886000	Enhancers	Small Intestine	intestine
15	chr7:16885800-16886200	Enhancers	Stomach Mucosa	stomach
16	chr7:16885800-16886400	Enhancers	Duodenum Mucosa	Duodenum
17	chr7:16885800-16886400	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr7:16885800-16886600	Enhancers	Fetal Brain Male	brain
19	chr7:16885800-16886800	Flanking Active TSS	A549	lung
20	chr7:16885800-16892600	Enhancers	Primary hematopoietic stem cells	blood
21	chr7:16886000-16886600	Weak transcription	Fetal Kidney	kidney
22	chr7:16886000-16886600	Enhancers	Rectal Mucosa Donor 29	rectum
23	chr7:16886000-16887200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr7:16886000-16889600	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr7:16886000-16900000	Weak transcription	Small Intestine	intestine
26	chr7:16886200-16886400	Enhancers	Placenta	Placenta
27	chr7:16886200-16886400	Flanking Active TSS	Stomach Mucosa	stomach
28	chr7:16886200-16886800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr7:16886200-16887400	Enhancers	Fetal Lung	lung
30	chr7:16886200-16887600	Flanking Active TSS	Hela-S3	cervix
31	chr7:16886200-16890400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:16886400-16886600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
33	chr7:16886400-16886800	Weak transcription	Placenta	Placenta
34	chr7:16886400-16887200	Enhancers	Stomach Mucosa	stomach
35	chr7:16886400-16887400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr7:16886400-16887600	Enhancers	NHEK	skin
37	chr7:16886400-16887800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:16886400-16889600	Weak transcription	Duodenum Mucosa	Duodenum
39	chr7:16886600-16886800	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
40	chr7:16886600-16887200	Active TSS	Rectal Mucosa Donor 31	rectum
41	chr7:16886600-16887400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr7:16886600-16887400	Enhancers	Fetal Kidney	kidney
43	chr7:16886600-16887400	Enhancers	HepG2	liver
44	chr7:16886600-16887600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr7:16886600-16890400	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr7:16886800-16887200	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr7:16886800-16887400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:16886800-16887400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:16886800-16887400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr7:16886800-16887400	Flanking Active TSS	Fetal Intestine Small	intestine

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