Variant report

Variant	esv3408073
Chromosome Location	chr6:74362256-74364804
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	chr6:74362319-74362991	HepG2	liver:	n/a	chr6:74362653-74362669
2	ARID3A	chr6:74361802-74362994	K562	blood:	n/a	chr6:74362653-74362669
3	ARID3A	chr6:74363690-74364032	K562	blood:	n/a	n/a
4	ARID3A	chr6:74363545-74364274	HepG2	liver:	n/a	n/a
5	ATF2	chr6:74363558-74363988	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr6:74363804-74364276	GM12878	blood:	n/a	n/a
7	ATF3	chr6:74362908-74363139	K562	blood:	n/a	n/a
8	BACH1	chr6:74363514-74363688	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr6:74362338-74362498	K562	blood:	n/a	n/a
10	BCL3	chr6:74363631-74364164	GM12878	blood:	n/a	chr6:74363703-74363716 chr6:74363705-74363714 chr6:74363783-74363792 chr6:74363780-74363793 chr6:74363878-74363891
11	BCL3	chr6:74363769-74364265	A549	lung:	n/a	chr6:74363783-74363792 chr6:74363780-74363793 chr6:74363878-74363891
12	BCLAF1	chr6:74363432-74364249	GM12878	blood:	n/a	chr6:74363460-74363469 chr6:74363703-74363716 chr6:74363705-74363714 chr6:74363783-74363792 chr6:74363780-74363793 chr6:74363878-74363891
13	BHLHE40	chr6:74362437-74362587	K562	blood:	n/a	n/a
14	BHLHE40	chr6:74363535-74364297	HepG2	liver:	n/a	chr6:74363694-74363710
15	BHLHE40	chr6:74362806-74364143	K562	blood:	n/a	chr6:74363198-74363214 chr6:74363404-74363420 chr6:74363694-74363710
16	BHLHE40	chr6:74363625-74364301	GM12878	blood:	n/a	chr6:74363694-74363710
17	BHLHE40	chr6:74364411-74365419	K562	blood:	n/a	chr6:74364877-74364898
18	BHLHE40	chr6:74364013-74364213	A549	lung:	n/a	n/a
19	BHLHE40	chr6:74364747-74365042	GM12878	blood:	n/a	chr6:74364877-74364898
20	BHLHE40	chr6:74362366-74363307	GM12878	blood:	n/a	chr6:74363198-74363214
21	BRCA1	chr6:74363602-74363991	HepG2	liver:	n/a	n/a
22	BRCA1	chr6:74363480-74363939	GM12878	blood:	n/a	n/a
23	BRCA1	chr6:74363669-74364007	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr6:74362322-74363128	Hela-S3	cervix:	n/a	n/a
25	CBX3	chr6:74363656-74364435	K562	blood:	n/a	n/a
26	CBX3	chr6:74362791-74363205	K562	blood:	n/a	n/a
27	CCNT2	chr6:74362748-74364091	K562	blood:	n/a	n/a
28	CEBPB	chr6:74363961-74364379	HepG2	liver:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
29	CEBPB	chr6:74363707-74364526	MCF-7	breast:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
30	CEBPB	chr6:74363747-74364464	HepG2	liver:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
31	CEBPB	chr6:74363911-74364383	K562	blood:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
32	CEBPB	chr6:74363580-74364458	H1-hESC	embryonic stem cell:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
33	CEBPB	chr6:74363879-74364369	HepG2	liver:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
34	CEBPB	chr6:74363492-74364460	HepG2	liver:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
35	CEBPB	chr6:74363777-74364388	GM12878	blood:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
36	CEBPB	chr6:74363583-74364651	Hela-S3	cervix:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
37	CEBPB	chr6:74363701-74364511	K562	blood:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
38	CEBPB	chr6:74363730-74364451	A549	lung:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
39	CEBPB	chr6:74363956-74364462	ECC-1	luminal epithelium:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
40	CEBPB	chr6:74363514-74364519	ECC-1	luminal epithelium:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
41	CEBPB	chr6:74363897-74364507	A549	lung:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
42	CEBPB	chr6:74363779-74364460	K562	blood:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
43	CEBPB	chr6:74363703-74364527	A549	lung:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
44	CEBPB	chr6:74363756-74364459	IMR90	lung:	n/a	chr6:74364269-74364280 chr6:74364076-74364089
45	CEBPD	chr6:74364104-74364399	HepG2	liver:	n/a	n/a
46	CEBPD	chr6:74363535-74364402	HepG2	liver:	n/a	chr6:74364077-74364088
47	CHD1	chr6:74362421-74363100	GM12878	blood:	n/a	n/a
48	CHD1	chr6:74363405-74364193	GM12878	blood:	n/a	n/a
49	CHD2	chr6:74363399-74364225	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr6:74362825-74364379	Hela-S3	cervix:	n/a	chr6:74363389-74363399

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74364667-74364717	Jurkat	blood:	n/a
2	chr6:74364700-74364750	HEEpiC	esophagus:	n/a
3	chr6:74363913-74363963	SAEC	small airway:	n/a
4	chr6:74363837-74363887	HRE	kidney:	n/a
5	chr6:74363913-74363963	PFSK-1	brain:	n/a
6	chr6:74363634-74363684	MCF-7	breast:	n/a
7	chr6:74364667-74364717	AG10803	skin:	n/a
8	chr6:74364149-74364199	HL-60	blood:	n/a
9	chr6:74363598-74363648	NHBE	bronchial:	n/a
10	chr6:74364149-74364199	NH-A	brain:	n/a
11	chr6:74363837-74363887	HUVEC	blood vessel:	n/a
12	chr6:74364667-74364717	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:74363634-74363684	HRE	kidney:	n/a
14	chr6:74364667-74364717	HRCEpiC	kidney:	n/a
15	chr6:74363634-74363684	BJ	skin:	n/a
16	chr6:74363775-74363825	HCPEpiC	choroid plexus:	n/a
17	chr6:74364700-74364750	HAEpiC	amniotic membrane:	n/a
18	chr6:74363775-74363825	HIPEpiC	eye:	n/a
19	chr6:74363634-74363684	Jurkat	blood:	n/a
20	chr6:74363775-74363825	SK-N-MC	brain:	n/a
21	chr6:74364667-74364717	HEEpiC	esophagus:	n/a
22	chr6:74364700-74364750	GM06990	blood:	n/a
23	chr6:74363837-74363887	ovcar-3	ovarian:	n/a
24	chr6:74364700-74364750	HCF	heart:	n/a
25	chr6:74363913-74363963	Hela-S3	cervix:	n/a
26	chr6:74364149-74364199	CMK	blood:	n/a
27	chr6:74363018-74363068	BE2_C	brain:	n/a
28	chr6:74364667-74364717	MCF-7	breast:	n/a
29	chr6:74363634-74363684	AG09309	skin:	n/a
30	chr6:74364667-74364717	ECC-1	luminal epithelium:	n/a
31	chr6:74363837-74363887	AG10803	skin:	n/a
32	chr6:74363018-74363068	PFSK-1	brain:	n/a
33	chr6:74363449-74363499	AG04449	skin:	fetal
34	chr6:74363888-74363938	AG04449	skin:	fetal
35	chr6:74364149-74364199	GM12878	blood:	n/a
36	chr6:74363879-74363929	SK-N-SH_RA	brain:	n/a
37	chr6:74364149-74364199	GM12892	blood:	n/a
38	chr6:74363884-74363934	T-47D	breast:	n/a
39	chr6:74363449-74363499	ECC-1	luminal epithelium:	n/a
40	chr6:74363775-74363825	NHDF-neo	bronchial:	n/a
41	chr6:74363879-74363929	K562	blood:	n/a
42	chr6:74363634-74363684	T-47D	breast:	n/a
43	chr6:74363884-74363934	NH-A	brain:	n/a
44	chr6:74363598-74363648	PANC-1	pancreas:	n/a
45	chr6:74363879-74363929	AG10803	skin:	n/a
46	chr6:74363018-74363068	HMEC	breast:	n/a
47	chr6:74363598-74363648	SK-N-SH	brain:	n/a
48	chr6:74363913-74363963	HL-60	blood:	n/a
49	chr6:74364667-74364717	NH-A	brain:	n/a
50	chr6:74363449-74363499	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:74228702..74232744-chr6:74360665..74366385,13	MCF-7	breast:
2	chr5:39073740..39074512-chr6:74363188..74364025,2	Hela-S3	cervix:
3	chr6:74219718..74234750-chr6:74354945..74369231,56	K562	blood:
4	chr6:74363322..74365404-chr6:75950708..75953547,2	MCF-7	breast:
5	chr6:74353596..74359738-chr6:74361541..74364786,8	MCF-7	breast:
6	chr14:35871636..35873724-chr6:74363774..74365365,2	MCF-7	breast:
7	chr6:74351063..74355074-chr6:74360720..74363620,5	K562	blood:
8	chr6:74170014..74172890-chr6:74363161..74365164,3	K562	blood:
9	chr6:74234985..74236932-chr6:74360713..74363466,3	K562	blood:
10	chr6:74229968..74230929-chr6:74362111..74362922,2	MCF-7	breast:
11	chr6:74230161..74230802-chr6:74362026..74362576,2	Hela-S3	cervix:
12	chr14:74180498..74181170-chr6:74363307..74364061,2	Hela-S3	cervix:
13	chr6:74103315..74106293-chr6:74362194..74365078,3	MCF-7	breast:
14	chr6:74225088..74225957-chr6:74362036..74362739,2	K562	blood:
15	chr6:74354143..74358709-chr6:74361254..74364709,5	MCF-7	breast:
16	chr6:74220976..74234980-chr6:74352572..74366941,62	K562	blood:
17	chr6:74228067..74234767-chr6:74357105..74365312,16	MCF-7	breast:
18	chr6:74362119..74363006-chr6:74442455..74443360,3	MCF-7	breast:
19	chr19:1591885..1592846-chr6:74363577..74364084,2	Hela-S3	cervix:
20	chr6:74159677..74160348-chr6:74362071..74362615,2	MCF-7	breast:
21	chr6:74169971..74171514-chr6:74363161..74365275,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CD109-1	chr6:74364304-74364586	XLOC_005347
2	lnc-CD109-1	chr6:74364303-74364586	NONHSAT113578

Variant related genes	Relation type
SLC17A5	TF binding region
SLC17A5	CpG island
ENSG00000164327	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000119899	chromatin interactions
ENSG00000112695	chromatin interactions
ENSG00000203907	chromatin interactions
ENSG00000229862	chromatin interactions
ENSG00000176903	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000223967	chromatin interactions
ENSG00000080007	chromatin interactions
ENSG00000071655	chromatin interactions
ENSG00000238464	chromatin interactions
ENSG00000156508	chromatin interactions

Extended variants
information (count: 95 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:95 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542162119	chr6:74362257-74362258	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs12189647	chr6:74362260-74362261	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs372499470	chr6:74362268-74362269	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs189491789	chr6:74362365-74362366	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs540190239	chr6:74362388-74362389	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs12203363	chr6:74362415-74362416	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs532218881	chr6:74362454-74362455	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs201950060	chr6:74362462-74362463	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs370100851	chr6:74362493-74362494	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs35469540	chr6:74362509-74362510	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs142689236	chr6:74362585-74362586	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs575296346	chr6:74362586-74362587	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs548140079	chr6:74362645-74362646	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs542311142	chr6:74362660-74362661	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs554253694	chr6:74362688-74362689	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs566380428	chr6:74362718-74362719	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs534485003	chr6:74362733-74362734	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs572666898	chr6:74362766-74362767	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs117078621	chr6:74362797-74362798	Active TSS Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs77876662	chr6:74362836-74362837	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs3839494	chr6:74362847-74362848	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs3799288	chr6:74362900-74362901	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs116414522	chr6:74362931-74362932	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs569613389	chr6:74363010-74363011	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs180971607	chr6:74363149-74363150	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
26	rs541977118	chr6:74363156-74363157	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
27	rs554119001	chr6:74363160-74363161	Active TSS Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs572374117	chr6:74363206-74363207	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs541764103	chr6:74363222-74363223	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
30	rs540516377	chr6:74363325-74363326	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
31	rs564874265	chr6:74363370-74363371	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Bivalent/Poised TSS	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
32	rs113203791	chr6:74363421-74363422	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
33	rs545374734	chr6:74363437-74363438	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
34	rs540961859	chr6:74363452-74363453	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
35	rs375009332	chr6:74363485-74363486	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs529760022	chr6:74363489-74363490	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs563578096	chr6:74363523-74363524	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs141463026	chr6:74363525-74363526	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs201942170	chr6:74363566-74363567	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs150836846	chr6:74363571-74363572	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
41	rs139255194	chr6:74363577-74363578	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs368359854	chr6:74363589-74363590	Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
43	rs372127642	chr6:74363601-74363602	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
44	rs374582872	chr6:74363604-74363605	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
45	rs552161786	chr6:74363640-74363641	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
46	rs571112994	chr6:74363656-74363657	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
47	rs538563117	chr6:74363677-74363678	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
48	rs550366773	chr6:74363681-74363682	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
49	rs530934473	chr6:74363718-74363719	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
50	rs370619209	chr6:74363742-74363743	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Ependymoma	16718352	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:74307200-74362400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:74314200-74362800	Weak transcription	Stomach Mucosa	stomach
3	chr6:74315600-74362800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:74324600-74362800	Weak transcription	Pancreas	Pancrea
5	chr6:74325400-74362800	Weak transcription	Small Intestine	intestine
6	chr6:74339200-74362800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr6:74341600-74362800	Weak transcription	Esophagus	oesophagus
8	chr6:74341600-74362800	Weak transcription	Gastric	stomach
9	chr6:74341800-74362600	Weak transcription	Brain Substantia Nigra	brain
10	chr6:74342000-74362800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr6:74342400-74362800	Weak transcription	Lung	lung
12	chr6:74342400-74362800	Weak transcription	Spleen	Spleen
13	chr6:74343200-74362600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:74347200-74362800	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr6:74349600-74362800	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr6:74350600-74362600	Weak transcription	Fetal Heart	heart
17	chr6:74351600-74362400	Weak transcription	Right Ventricle	heart
18	chr6:74355600-74362400	Weak transcription	Primary B cells from peripheral blood	blood
19	chr6:74355600-74362400	Weak transcription	Thymus	Thymus
20	chr6:74355600-74362800	Weak transcription	Left Ventricle	heart
21	chr6:74355800-74362400	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr6:74355800-74362400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr6:74355800-74362400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
24	chr6:74355800-74362400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:74355800-74362400	Weak transcription	Brain Angular Gyrus	brain
26	chr6:74355800-74362400	Weak transcription	Brain Cingulate Gyrus	brain
27	chr6:74355800-74362400	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr6:74355800-74362400	Weak transcription	Fetal Thymus	thymus
29	chr6:74355800-74362400	Weak transcription	Psoas Muscle	Psoas
30	chr6:74355800-74362600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr6:74355800-74362600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr6:74355800-74362600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr6:74355800-74362600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr6:74355800-74362600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr6:74355800-74362600	Weak transcription	Fetal Brain Male	brain
36	chr6:74355800-74362800	Weak transcription	Colonic Mucosa	Colon
37	chr6:74355800-74362800	Weak transcription	Ovary	ovary
38	chr6:74356000-74362400	Weak transcription	Stomach Smooth Muscle	stomach
39	chr6:74356200-74362600	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr6:74357200-74362600	Weak transcription	Aorta	Aorta
41	chr6:74358400-74362400	Weak transcription	HMEC	breast
42	chr6:74358600-74362400	Weak transcription	Fetal Kidney	kidney
43	chr6:74358600-74362600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:74358600-74362600	Weak transcription	HSMM	muscle
45	chr6:74359800-74362400	Weak transcription	Rectal Mucosa Donor 31	rectum
46	chr6:74359800-74362400	Weak transcription	Skeletal Muscle Female	skeletal muscle
47	chr6:74359800-74362600	Weak transcription	Placenta	Placenta
48	chr6:74359800-74362800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr6:74360000-74362400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr6:74360000-74362400	Weak transcription	Fetal Muscle Trunk	muscle

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