Variant report

Variant	esv3376987
Chromosome Location	chr17:18086452-18089000
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:18086179-18087063	K562	blood:	n/a	n/a
2	ARID3A	chr17:18086352-18087217	HepG2	liver:	n/a	n/a
3	ATF1	chr17:18086200-18087306	K562	blood:	n/a	chr17:18087187-18087201
4	ATF2	chr17:18086102-18087310	GM12878	blood:	n/a	chr17:18087187-18087201
5	ATF2	chr17:18086254-18087079	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr17:18086240-18087051	GM12878	blood:	n/a	n/a
7	ATF2	chr17:18086850-18087300	H1-hESC	embryonic stem cell:	n/a	chr17:18087187-18087201
8	ATF3	chr17:18086848-18087182	K562	blood:	n/a	chr17:18086949-18086958
9	ATF3	chr17:18086796-18087171	K562	blood:	n/a	chr17:18086949-18086958
10	ATF3	chr17:18086249-18087333	A549	lung:	n/a	chr17:18086949-18086958 chr17:18087188-18087201
11	ATF3	chr17:18086143-18087340	A549	lung:	n/a	chr17:18086949-18086958 chr17:18087188-18087201
12	BACH1	chr17:18087983-18088669	K562	blood:	n/a	n/a
13	BACH1	chr17:18086157-18088472	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr17:18086197-18087064	K562	blood:	n/a	n/a
15	BCL11A	chr17:18086469-18086839	GM12878	blood:	n/a	n/a
16	BCL11A	chr17:18086454-18087087	GM12878	blood:	n/a	chr17:18087015-18087024
17	BCL3	chr17:18085961-18087368	A549	lung:	n/a	chr17:18087015-18087024 chr17:18086418-18086431 chr17:18087277-18087286 chr17:18086410-18086423 chr17:18087302-18087315 chr17:18086409-18086422 chr17:18086407-18086420 chr17:18086408-18086417 chr17:18086416-18086429
18	BCL3	chr17:18087646-18088303	A549	lung:	n/a	n/a
19	BCL3	chr17:18086107-18087127	A549	lung:	n/a	chr17:18087015-18087024 chr17:18086418-18086431 chr17:18086410-18086423 chr17:18086409-18086422 chr17:18086407-18086420 chr17:18086408-18086417 chr17:18086416-18086429
20	BCLAF1	chr17:18086196-18087156	GM12878	blood:	n/a	chr17:18087015-18087024 chr17:18086418-18086431 chr17:18086410-18086423 chr17:18086409-18086422 chr17:18086407-18086420 chr17:18086408-18086417 chr17:18086416-18086429
21	BCLAF1	chr17:18086134-18087344	GM12878	blood:	n/a	chr17:18087015-18087024 chr17:18086418-18086431 chr17:18087277-18087286 chr17:18086410-18086423 chr17:18087302-18087315 chr17:18086409-18086422 chr17:18086407-18086420 chr17:18086408-18086417 chr17:18086416-18086429
22	BHLHE40	chr17:18085689-18087366	GM12878	blood:	n/a	chr17:18086407-18086423 chr17:18086495-18086511 chr17:18086410-18086426 chr17:18087270-18087286 chr17:18086415-18086431 chr17:18086404-18086420 chr17:18087295-18087311 chr17:18086399-18086415
23	BHLHE40	chr17:18087994-18088496	K562	blood:	n/a	n/a
24	BHLHE40	chr17:18086206-18087403	K562	blood:	n/a	chr17:18086407-18086423 chr17:18086495-18086511 chr17:18086410-18086426 chr17:18087270-18087286 chr17:18086415-18086431 chr17:18086404-18086420 chr17:18087295-18087311 chr17:18086399-18086415
25	BRCA1	chr17:18087921-18089168	Hela-S3	cervix:	n/a	chr17:18088984-18088991
26	BRCA1	chr17:18086252-18087321	HepG2	liver:	n/a	n/a
27	BRCA1	chr17:18086199-18087468	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr17:18085987-18087458	GM12878	blood:	n/a	n/a
29	CBX3	chr17:18087904-18088329	K562	blood:	n/a	n/a
30	CCNT2	chr17:18086198-18088353	K562	blood:	n/a	chr17:18087009-18087018
31	CEBPB	chr17:18086404-18087163	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr17:18086180-18087309	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr17:18086542-18087106	HepG2	liver:	n/a	n/a
34	CEBPB	chr17:18086645-18087065	K562	blood:	n/a	n/a
35	CEBPD	chr17:18086152-18087464	HepG2	liver:	n/a	n/a
36	CHD1	chr17:18087735-18088403	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD1	chr17:18085856-18091134	IMR90	lung:	n/a	n/a
38	CHD1	chr17:18086161-18089744	GM12878	blood:	n/a	n/a
39	CHD2	chr17:18086275-18087340	K562	blood:	n/a	n/a
40	CHD2	chr17:18085757-18088505	GM12878	blood:	n/a	n/a
41	CHD2	chr17:18087732-18087884	HepG2	liver:	n/a	n/a
42	CHD2	chr17:18086298-18087420	HepG2	liver:	n/a	n/a
43	CHD2	chr17:18088313-18088474	HepG2	liver:	n/a	n/a
44	CHD2	chr17:18086185-18087441	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr17:18086153-18088514	Hela-S3	cervix:	n/a	n/a
46	CHD2	chr17:18087883-18087969	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chr17:18086271-18087306	A549	lung:	n/a	n/a
48	CREB1	chr17:18087808-18088380	K562	blood:	n/a	n/a
49	CREB1	chr17:18087836-18088455	HepG2	liver:	n/a	n/a
50	CREB1	chr17:18087820-18088412	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:18088359-18088409	GM12892	blood:	n/a
2	chr17:18088359-18088409	GM12892	blood:	n/a
3	chr17:18086863-18086913	HCF	heart:	n/a
4	chr17:18086957-18087007	GM12878	blood:	n/a
5	chr17:18086721-18086771	GM12878	blood:	n/a
6	chr17:18086559-18086609	HRPEpiC	eye:	n/a
7	chr17:18086863-18086913	NHDF-neo	bronchial:	n/a
8	chr17:18086837-18086887	Hepatocyte	liver:	n/a
9	chr17:18088095-18088145	MCF10A-Er-Src	breast:	n/a
10	chr17:18086889-18086939	PFSK-1	brain:	n/a
11	chr17:18086889-18086939	HUVEC	blood vessel:	n/a
12	chr17:18086444-18086494	HMEC	breast:	n/a
13	chr17:18086837-18086887	GM19239	blood:	n/a
14	chr17:18086889-18086939	Hepatocyte	liver:	n/a
15	chr17:18088095-18088145	BJ	skin:	n/a
16	chr17:18086444-18086494	AG04450	lung:	fetal
17	chr17:18086714-18086764	HL-60	blood:	n/a
18	chr17:18088095-18088145	T-47D	breast:	n/a
19	chr17:18086859-18086909	ECC-1	luminal epithelium:	n/a
20	chr17:18086559-18086609	GM12891	blood:	n/a
21	chr17:18087255-18087305	BJ	skin:	n/a
22	chr17:18086957-18087007	U87	brain:	n/a
23	chr17:18086957-18087007	HL-60	blood:	n/a
24	chr17:18086721-18086771	MCF-7	breast:	n/a
25	chr17:18087580-18087630	ProgFib	skin:	n/a
26	chr17:18086444-18086494	A549	lung:	n/a
27	chr17:18086444-18086494	LNCaP	prostate:	n/a
28	chr17:18088549-18088599	HNPCEpiC	eye:	n/a
29	chr17:18086863-18086913	HEK293	kidney:	embryo
30	chr17:18087255-18087305	RPTEC	kidney:	n/a
31	chr17:18086957-18087007	HCPEpiC	choroid plexus:	n/a
32	chr17:18087580-18087630	HRPEpiC	eye:	n/a
33	chr17:18087255-18087305	NB4	blood:	n/a
34	chr17:18086889-18086939	Hela-S3	cervix:	n/a
35	chr17:18087255-18087305	AoSMC	blood vessel:	n/a
36	chr17:18087255-18087305	HCM	heart:	n/a
37	chr17:18086859-18086909	GM12892	blood:	n/a
38	chr17:18086472-18086522	H1-hESC	embryonic stem cell:	embryo
39	chr17:18086863-18086913	NT2-D1	testis:	n/a
40	chr17:18088095-18088145	IMR90	lung:	fetal
41	chr17:18088359-18088409	HepG2	liver:	n/a
42	chr17:18088359-18088409	Hepatocyte	liver:	n/a
43	chr17:18086957-18087007	HCM	heart:	n/a
44	chr17:18086472-18086522	HCF	heart:	n/a
45	chr17:18087255-18087305	HepG2	liver:	n/a
46	chr17:18086721-18086771	SK-N-SH_RA	brain:	n/a
47	chr17:18086889-18086939	AG04450	lung:	fetal
48	chr17:18086559-18086609	Hela-S3	cervix:	n/a
49	chr17:18086863-18086913	GM06990	blood:	n/a
50	chr17:18086472-18086522	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr17:18063606..18070028-chr17:18081885..18087934,10	MCF-7	breast:
2	chr17:18085249..18088032-chr17:18163903..18166046,2	MCF-7	breast:
3	chr17:18085295..18087427-chr9:125026325..125027854,2	MCF-7	breast:
4	chr17:18085097..18087844-chr17:18150702..18152403,2	MCF-7	breast:
5	chr17:18061742..18067292-chr17:18083221..18089651,7	K562	blood:
6	chr11:62608619..62609399-chr17:18085958..18086713,2	Hela-S3	cervix:
7	chr17:18059406..18063498-chr17:18086302..18089651,4	K562	blood:
8	chr17:18086032..18088176-chr17:18160313..18162937,3	K562	blood:
9	chr17:18057350..18061680-chr17:18083813..18088656,8	K562	blood:
10	chr17:18086084..18087983-chr17:18217517..18220819,3	MCF-7	breast:
11	chr17:18057503..18062681-chr17:18084968..18089396,8	MCF-7	breast:
12	chr17:18085197..18089449-chr17:18160313..18164902,6	K562	blood:
13	chr17:18088851..18092330-chr17:18106978..18109728,3	K562	blood:
14	chr17:18085827..18086663-chr5:115177264..115177884,2	Hela-S3	cervix:
15	chr17:18086297..18088229-chr17:18161732..18163616,2	MCF-7	breast:
16	chr17:18088345..18089995-chr17:18161627..18163535,2	K562	blood:
17	chr17:18088174..18090098-chr17:18107695..18110027,2	MCF-7	breast:
18	chr17:18086116..18088007-chr17:18126945..18129861,2	K562	blood:
19	chr17:18087075..18087717-chr22:46692104..46692982,2	NB4	blood:
20	chr17:18085788..18088045-chr17:18160400..18163100,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FLII-3	chr17:18088550-18088914	predAs_chen_AI570526_1
2	lnc-FLII-1	chr17:18087711-18088067	ENSG00000246628
3	lnc-FLII-1	chr17:18087711-18087981	ENSG00000266677.1

Variant related genes	Relation type
ALKBH5	TF binding region
ENSG00000266677	TF binding region
ALKBH5	CpG island
ENSG00000266677	CpG island
ENSG00000091536	chromatin interactions
ENSG00000148187	chromatin interactions
ENSG00000177731	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000176994	chromatin interactions
ENSG00000145782	chromatin interactions
ENSG00000177427	chromatin interactions
ENSG00000177879	chromatin interactions
ENSG00000119446	chromatin interactions
ENSG00000177302	chromatin interactions
ENSG00000131899	chromatin interactions
ENSG00000075218	chromatin interactions
ENSG00000091542	chromatin interactions
IL12A	miRNA target sites

Extended variants
information (count: 113 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:113 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533899501	chr17:18086461-18086462	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
2	rs553899111	chr17:18086491-18086492	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
3	rs78123366	chr17:18086495-18086496	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
4	rs374650339	chr17:18086537-18086538	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
5	rs536249133	chr17:18086560-18086561	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
6	rs552236280	chr17:18086570-18086571	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
7	rs576304295	chr17:18086575-18086576	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
8	rs199976799	chr17:18086590-18086591	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
9	rs544889901	chr17:18086636-18086637	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
10	rs34769216	chr17:18086701-18086702	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
11	rs558358916	chr17:18086716-18086717	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs368070273	chr17:18086765-18086766	Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs540370050	chr17:18086780-18086781	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs74874812	chr17:18086790-18086791	Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs568940176	chr17:18086813-18086814	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs144922193	chr17:18086820-18086821	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs375014787	chr17:18086823-18086824	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs574002679	chr17:18086844-18086845	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs543028400	chr17:18086860-18086861	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs111717461	chr17:18086876-18086877	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs562705500	chr17:18086917-18086918	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs537961972	chr17:18086931-18086932	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs146551631	chr17:18086951-18086952	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs184032516	chr17:18086963-18086964	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs565522340	chr17:18086964-18086965	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs369829979	chr17:18086985-18086986	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs7210578	chr17:18087015-18087016	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs527875969	chr17:18087030-18087031	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs547631329	chr17:18087038-18087039	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs113194255	chr17:18087047-18087048	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
31	rs567378942	chr17:18087055-18087056	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
32	rs141283755	chr17:18087061-18087062	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
33	rs549785326	chr17:18087084-18087085	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs113929888	chr17:18087085-18087086	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs568647283	chr17:18087102-18087103	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs371879130	chr17:18087129-18087130	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs538595406	chr17:18087147-18087148	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs558421254	chr17:18087167-18087168	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs571970012	chr17:18087182-18087183	Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs552269862	chr17:18087217-18087218	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs375227400	chr17:18087291-18087292	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs1064629	chr17:18087299-18087300	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs372908110	chr17:18087424-18087425	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
44	rs554438914	chr17:18087495-18087496	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
45	rs574095180	chr17:18087519-18087520	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
46	rs143278496	chr17:18087552-18087553	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs377071193	chr17:18087737-18087738	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
48	rs370188460	chr17:18087755-18087756	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
49	rs61999283	chr17:18087756-18087757	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a
50	rs564158465	chr17:18087783-18087784	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Weak transcription	Chromatin interactive region lncRNA	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:161)

Disease	PMID	Source
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
Melanoma	18172304	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
Oral squamous cell carcinoma	17134496	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
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	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
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Sezary syndrome	18413736	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Smith-Magenis syndrome	22283845	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:365 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18085600-18086600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr17:18085600-18086600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr17:18085600-18088600	Active TSS	iPS-20b Cell Line	embryonic stem cell
4	chr17:18085600-18088800	Active TSS	H9 Cell Line	embryonic stem cell
5	chr17:18085600-18088800	Active TSS	HUES64 Cell Line	embryonic stem cell
6	chr17:18085600-18089000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr17:18085600-18090600	Active TSS	Aorta	Aorta
8	chr17:18085800-18086600	Flanking Active TSS	Primary B cells from cord blood	blood
9	chr17:18085800-18086600	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr17:18085800-18086600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
11	chr17:18085800-18087000	Active TSS	Stomach Mucosa	stomach
12	chr17:18085800-18088000	Active TSS	H1 Cell Line	embryonic stem cell
13	chr17:18085800-18088000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr17:18085800-18088000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr17:18085800-18088000	Active TSS	Esophagus	oesophagus
16	chr17:18085800-18088200	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr17:18085800-18088400	Active TSS	HUES48 Cell Line	embryonic stem cell
18	chr17:18085800-18088800	Active TSS	Fetal Kidney	kidney
19	chr17:18085800-18088800	Active TSS	Psoas Muscle	Psoas
20	chr17:18085800-18089000	Active TSS	ES-I3 Cell Line	embryonic stem cell
21	chr17:18085800-18089000	Active TSS	Small Intestine	intestine
22	chr17:18085800-18089200	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr17:18085800-18089400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr17:18085800-18090200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
25	chr17:18085800-18090600	Active TSS	Pancreatic Islets	Pancreatic Islet
26	chr17:18086000-18087400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
27	chr17:18086000-18087400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr17:18086000-18087800	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr17:18086000-18087800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr17:18086000-18087800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr17:18086000-18087800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr17:18086000-18087800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr17:18086000-18087800	Active TSS	Fetal Stomach	stomach
34	chr17:18086000-18087800	Active TSS	Rectal Mucosa Donor 29	rectum
35	chr17:18086000-18087800	Active TSS	Skeletal Muscle Male	skeletal muscle
36	chr17:18086000-18087800	Active TSS	Skeletal Muscle Female	skeletal muscle
37	chr17:18086000-18087800	Active TSS	Dnd41	blood
38	chr17:18086000-18087800	Active TSS	HepG2	liver
39	chr17:18086000-18087800	Active TSS	Monocytes-CD14+_RO01746	blood
40	chr17:18086000-18088000	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr17:18086000-18088000	Active TSS	Liver	Liver
42	chr17:18086000-18088000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
43	chr17:18086000-18088000	Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr17:18086000-18088000	Active TSS	Fetal Intestine Small	intestine
45	chr17:18086000-18088000	Active TSS	Placenta Amnion	Placenta Amnion
46	chr17:18086000-18088000	Active TSS	Rectal Mucosa Donor 31	rectum
47	chr17:18086000-18088000	Active TSS	Right Ventricle	heart
48	chr17:18086000-18088200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr17:18086000-18088200	Active TSS	Primary T cells from cord blood	blood
50	chr17:18086000-18088200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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