Variant report

Variant	nsv830607
Chromosome Location	chr6:23302325-23446497
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	ATF1	chr6:23387787-23387921	K562	blood:	n/a	n/a
2	ATF1	chr6:23338418-23338445	K562	blood:	n/a	n/a
3	ATF2	chr6:23415968-23416511	GM12878	blood:	n/a	n/a
4	ATF2	chr6:23414135-23414644	GM12878	blood:	n/a	n/a
5	ATF2	chr6:23416106-23416567	GM12878	blood:	n/a	n/a
6	BACH1	chr6:23419141-23419147	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr6:23416053-23416435	GM12878	blood:	n/a	n/a
8	BATF	chr6:23415983-23416392	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:23416069-23416370	GM12878	blood:	n/a	n/a
10	BCL3	chr6:23414309-23414667	GM12878	blood:	n/a	chr6:23414525-23414534
11	BCL3	chr6:23303369-23303621	GM12878	blood:	n/a	n/a
12	BHLHE40	chr6:23409671-23409961	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:23414203-23414578	GM12878	blood:	n/a	n/a
14	CEBPB	chr6:23320930-23321169	H1-hESC	embryonic stem cell:	n/a	chr6:23321010-23321021 chr6:23321010-23321019 chr6:23321008-23321019 chr6:23321008-23321021 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321008-23321021
15	CEBPB	chr6:23440350-23440658	HepG2	liver:	n/a	chr6:23440489-23440500
16	CEBPB	chr6:23320876-23321193	A549	lung:	n/a	chr6:23321010-23321021 chr6:23321010-23321019 chr6:23321008-23321019 chr6:23321008-23321021 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321008-23321021
17	CEBPB	chr6:23390499-23390835	HepG2	liver:	n/a	chr6:23390666-23390679 chr6:23390668-23390677 chr6:23390666-23390677 chr6:23390668-23390677 chr6:23390668-23390677 chr6:23390666-23390679 chr6:23390668-23390679 chr6:23390668-23390679 chr6:23390666-23390679 chr6:23390668-23390677
18	CEBPB	chr6:23330894-23331217	ECC-1	luminal epithelium:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
19	CEBPB	chr6:23403672-23403995	MCF-7	breast:	n/a	n/a
20	CEBPB	chr6:23330914-23331303	MCF-7	breast:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
21	CEBPB	chr6:23318176-23318409	HepG2	liver:	n/a	chr6:23318253-23318264
22	CEBPB	chr6:23330895-23331225	MCF-7	breast:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
23	CEBPB	chr6:23334355-23334638	HepG2	liver:	n/a	chr6:23334482-23334493
24	CEBPB	chr6:23320866-23321156	K562	blood:	n/a	chr6:23321010-23321021 chr6:23321010-23321019 chr6:23321008-23321019 chr6:23321008-23321021 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321008-23321021
25	CEBPB	chr6:23415930-23416493	GM12878	blood:	n/a	n/a
26	CEBPB	chr6:23330894-23331260	ECC-1	luminal epithelium:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
27	CEBPB	chr6:23330885-23331213	Hela-S3	cervix:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
28	CEBPB	chr6:23320833-23321195	IMR90	lung:	n/a	chr6:23321010-23321021 chr6:23321010-23321019 chr6:23321008-23321019 chr6:23321008-23321021 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321008-23321021
29	CEBPB	chr6:23330911-23331234	A549	lung:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
30	CEBPB	chr6:23320893-23321164	MCF-7	breast:	n/a	chr6:23321010-23321021 chr6:23321010-23321019 chr6:23321008-23321019 chr6:23321008-23321021 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321008-23321021
31	CEBPB	chr6:23330878-23331253	IMR90	lung:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
32	CEBPB	chr6:23440425-23440607	Hela-S3	cervix:	n/a	chr6:23440489-23440500
33	CEBPB	chr6:23338596-23338876	HepG2	liver:	n/a	chr6:23338729-23338740 chr6:23338728-23338741
34	CEBPB	chr6:23440436-23440599	A549	lung:	n/a	chr6:23440489-23440500
35	CEBPB	chr6:23330882-23331245	HepG2	liver:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
36	CEBPB	chr6:23320841-23321195	HepG2	liver:	n/a	chr6:23321010-23321021 chr6:23321010-23321019 chr6:23321008-23321019 chr6:23321008-23321021 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321010-23321019 chr6:23321008-23321021
37	CEBPB	chr6:23330906-23331224	H1-hESC	embryonic stem cell:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
38	CEBPB	chr6:23390512-23390807	A549	lung:	n/a	chr6:23390666-23390679 chr6:23390668-23390677 chr6:23390666-23390677 chr6:23390668-23390677 chr6:23390668-23390677 chr6:23390666-23390679 chr6:23390668-23390679 chr6:23390668-23390679 chr6:23390666-23390679 chr6:23390668-23390677
39	CEBPB	chr6:23390536-23390818	IMR90	lung:	n/a	chr6:23390666-23390679 chr6:23390668-23390677 chr6:23390666-23390677 chr6:23390668-23390677 chr6:23390668-23390677 chr6:23390666-23390679 chr6:23390668-23390679 chr6:23390668-23390679 chr6:23390666-23390679 chr6:23390668-23390677
40	CEBPB	chr6:23330941-23331221	K562	blood:	n/a	chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331063-23331072 chr6:23331061-23331072 chr6:23331063-23331072
41	CEBPB	chr6:23374411-23374623	IMR90	lung:	n/a	n/a
42	CEBPB	chr6:23413632-23414192	IMR90	lung:	n/a	chr6:23414017-23414034 chr6:23414020-23414033
43	CHD2	chr6:23414418-23414581	GM12878	blood:	n/a	n/a
44	CTCF	chr6:23414700-23414850	HAc	cerebellar:	n/a	n/a
45	CTCF	chr6:23414520-23414670	AG10803	skin:	n/a	chr6:23414588-23414606
46	CTCF	chr6:23414540-23414690	HCM	heart:	n/a	chr6:23414588-23414606
47	CTCF	chr6:23414500-23414650	GM06990	blood:	n/a	chr6:23414588-23414606
48	CTCF	chr6:23414480-23414630	HEEpiC	esophagus:	n/a	chr6:23414588-23414606
49	CTCF	chr6:23414480-23414630	SK-N-SH_RA	brain:	n/a	chr6:23414588-23414606
50	CTCF	chr6:23414520-23414670	MCF-7	breast:	n/a	chr6:23414588-23414606

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:23408789-23408839	Hepatocyte	liver:	n/a
2	chr6:23397853-23397903	GM06990	blood:	n/a
3	chr6:23414372-23414422	IMR90	lung:	fetal
4	chr6:23414372-23414422	HUVEC	blood vessel:	n/a
5	chr6:23414372-23414422	HL-60	blood:	n/a
6	chr6:23408789-23408839	NH-A	brain:	n/a
7	chr6:23408789-23408839	PrEC	prostate:	n/a
8	chr6:23397853-23397903	NH-A	brain:	n/a
9	chr6:23414372-23414422	Hela-S3	cervix:	n/a
10	chr6:23414372-23414422	HRCEpiC	kidney:	n/a
11	chr6:23414372-23414422	SKMC	muscle:	n/a
12	chr6:23414372-23414422	AG10803	skin:	n/a
13	chr6:23408789-23408839	HL-60	blood:	n/a
14	chr6:23397853-23397903	HAEpiC	amniotic membrane:	n/a
15	chr6:23414372-23414422	ovcar-3	ovarian:	n/a
16	chr6:23408789-23408839	RPTEC	kidney:	n/a
17	chr6:23414372-23414422	AG09309	skin:	n/a
18	chr6:23414372-23414422	NHBE	bronchial:	n/a
19	chr6:23397853-23397903	HCF	heart:	n/a
20	chr6:23414372-23414422	HCM	heart:	n/a
21	chr6:23408789-23408839	ProgFib	skin:	n/a
22	chr6:23414372-23414422	PrEC	prostate:	n/a
23	chr6:23414372-23414422	RPTEC	kidney:	n/a
24	chr6:23414372-23414422	NHDF-neo	bronchial:	n/a
25	chr6:23397853-23397903	HNPCEpiC	eye:	n/a
26	chr6:23414372-23414422	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:23414372-23414422	HCF	heart:	n/a
28	chr6:23397853-23397903	AG04450	lung:	fetal
29	chr6:23414372-23414422	HCPEpiC	choroid plexus:	n/a
30	chr6:23397853-23397903	K562	blood:	n/a
31	chr6:23414372-23414422	A549	lung:	n/a
32	chr6:23414372-23414422	HNPCEpiC	eye:	n/a
33	chr6:23414372-23414422	BJ	skin:	n/a
34	chr6:23408789-23408839	BE2_C	brain:	n/a
35	chr6:23414372-23414422	AoSMC	blood vessel:	n/a
36	chr6:23408789-23408839	AG04450	lung:	fetal
37	chr6:23414372-23414422	GM12878	blood:	n/a
38	chr6:23397853-23397903	AoSMC	blood vessel:	n/a
39	chr6:23414372-23414422	SK-N-SH	brain:	n/a
40	chr6:23408789-23408839	SK-N-SH	brain:	n/a
41	chr6:23408789-23408839	HIPEpiC	eye:	n/a
42	chr6:23408789-23408839	SK-N-MC	brain:	n/a
43	chr6:23397853-23397903	T-47D	breast:	n/a
44	chr6:23414372-23414422	GM12891	blood:	n/a
45	chr6:23397853-23397903	Jurkat	blood:	n/a
46	chr6:23397853-23397903	AG04449	skin:	fetal
47	chr6:23414372-23414422	U87	brain:	n/a
48	chr6:23397853-23397903	PrEC	prostate:	n/a
49	chr6:23408789-23408839	GM12892	blood:	n/a
50	chr6:23414372-23414422	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:77050054..77050587-chr6:23338692..23339320,2	MCF-7	breast:
2	chr6:23317102..23318808-chr6:23319383..23321873,2	K562	blood:
3	chr6:23305391..23308000-chr6:23349016..23350977,2	MCF-7	breast:
4	chr6:23310938..23313547-chr6:23318215..23319852,2	MCF-7	breast:
5	chr6:23386279..23389198-chr6:23393366..23395282,2	K562	blood:
6	chr6:23381443..23383453-chr6:23386324..23390234,3	K562	blood:
7	chr6:23310938..23313547-chr6:23318215..23319852,2	MCF-7	breast:
8	chr6:23305391..23308000-chr6:23349016..23350977,2	MCF-7	breast:
9	chr6:23303590..23305358-chr6:23306673..23309551,2	K562	blood:
10	chr6:23324427..23327416-chr6:23329327..23331380,2	K562	blood:
11	chr6:23317102..23318808-chr6:23319383..23321873,2	K562	blood:
12	chr6:23324427..23327416-chr6:23329327..23331380,2	K562	blood:
13	chr6:23337667..23339611-chr6:23341451..23343030,2	K562	blood:
14	chr6:23386279..23389198-chr6:23393366..23395282,2	K562	blood:
15	chr6:23440575..23443295-chr6:23443874..23446854,2	K562	blood:
16	chr6:21602438..21605150-chr6:23415415..23417110,2	MCF-7	breast:
17	chr6:23381443..23383453-chr6:23386324..23390234,3	K562	blood:
18	chr6:23440575..23443295-chr6:23443874..23446854,2	K562	blood:
19	chr6:23303590..23305358-chr6:23306673..23309551,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRSN1-3	chr6:23349662-23349763	XLOC_005201
2	lnc-NRSN1-3	chr6:23351472-23351675	XLOC_005201
3	lnc-HDGFL1-5	chr6:23337939-23338024	ENSG00000235743
4	lnc-NRSN1-8	chr6:23395032-23395182	NONHSAT108095
5	lnc-HDGFL1-8	chr6:23347170-23347430	NONHSAT108092
6	lnc-NRSN1-2	chr6:23404092-23404250	XLOC_005202
7	lnc-NRSN1-1	chr6:23441808-23441894	XLOC_005203
8	lnc-NRSN1-2	chr6:23404092-23404502	XLOC_005202
9	lnc-HDGFL1-5	chr6:23346744-23346788	NONHSAT108090
10	lnc-NRSN1-8	chr6:23380002-23380135	NONHSAT108095
11	lnc-HDGFL1-5	chr6:23345100-23345355	NONHSAT108090
12	lnc-NRSN1-1	chr6:23416372-23416477	XLOC_005203
13	lnc-NRSN1-2	chr6:23399272-23399350	XLOC_005202
14	lnc-NRSN1-8	chr6:23397482-23397602	NONHSAT108095
15	lnc-NRSN1-1	chr6:23445918-23446003	NONHSAT108100
16	lnc-NRSN1-2	chr6:23403169-23403351	XLOC_005202
17	lnc-NRSN1-2	chr6:23399154-23399350	XLOC_005202
18	lnc-NRSN1-3	chr6:23370187-23370502	XLOC_005201
19	lnc-HDGFL1-5	chr6:23346744-23346788	ENSG00000235743
20	lnc-NRSN1-7	chr6:23438116-23439947	NONHSAT108099
21	lnc-HDGFL1-8	chr6:23347011-23347037	NONHSAT108092
22	lnc-DCDC2-1	chr6:23339488-23339917	NONHSAT108091
23	lnc-HDGFL1-5	chr6:23345178-23345248	ENSG00000235743
24	lnc-DCDC2-1	chr6:23338304-23338487	NONHSAT108091
25	lnc-HDGFL1-5	chr6:23337939-23338024	NONHSAT108090
26	lnc-HDGFL1-5	chr6:23341963-23342072	ENSG00000235743
27	lnc-HDGFL1-5	chr6:23341963-23342072	NONHSAT108090

Variant related genes	Relation type
ENSG00000235743	TF binding region
ENSG00000235743	CpG island
ENSG00000235743	chromatin interactions

Extended variants
information (count: 3018 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3018 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574843622	chr6:23302409-23302410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531695613	chr6:23302423-23302424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs561137724	chr6:23302492-23302493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs557339332	chr6:23302501-23302502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs186849422	chr6:23302508-23302509	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142775907	chr6:23302513-23302514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs553997519	chr6:23302529-23302530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs565836343	chr6:23302530-23302531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539768407	chr6:23302549-23302550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190156893	chr6:23302575-23302576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs113509745	chr6:23302592-23302593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs575990963	chr6:23302616-23302617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs542226311	chr6:23302619-23302620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs555219333	chr6:23302650-23302651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573672028	chr6:23302726-23302727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs76117864	chr6:23302758-23302759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560317847	chr6:23302790-23302791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs528586248	chr6:23302793-23302794	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544469440	chr6:23302796-23302797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369386069	chr6:23302797-23302798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs546104394	chr6:23302812-23302813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs368322122	chr6:23302813-23302814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs372018434	chr6:23302872-23302873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs147349265	chr6:23302887-23302888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541272334	chr6:23302908-23302909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs550144113	chr6:23302928-23302929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs562079387	chr6:23302942-23302943	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs559541868	chr6:23302943-23302944	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs188771282	chr6:23302947-23302948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79718902	chr6:23302974-23302975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs539630146	chr6:23303005-23303006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs551416812	chr6:23303007-23303008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs7751274	chr6:23303015-23303016	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs536689072	chr6:23303045-23303046	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs148411392	chr6:23303048-23303049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs116738945	chr6:23303087-23303088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs534433017	chr6:23303096-23303097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs372369425	chr6:23303104-23303105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs80332357	chr6:23303106-23303107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572339137	chr6:23303133-23303134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs193069954	chr6:23303150-23303151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564671816	chr6:23303155-23303156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs576662510	chr6:23303160-23303161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs543715037	chr6:23303167-23303168	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370251763	chr6:23303184-23303185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562113451	chr6:23303202-23303203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs375718832	chr6:23303274-23303275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529273423	chr6:23303277-23303278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs185846520	chr6:23303337-23303338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs142444604	chr6:23303373-23303374	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial cell carcinoma	18451213	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian cancer	20844748	CNVD
Developmental delay	19490664	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Tetralogy of Fallot	22912587	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:23302400-23303600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr6:23302600-23303400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr6:23302800-23303600	Enhancers	HUVEC	blood vessel
4	chr6:23303400-23303600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:23305400-23306200	Enhancers	Liver	Liver
6	chr6:23306200-23307800	Weak transcription	Liver	Liver
7	chr6:23306400-23307000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:23306600-23306800	Enhancers	NHEK	skin
9	chr6:23306600-23307200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr6:23307000-23308600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr6:23307200-23308400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr6:23307800-23308000	Enhancers	Liver	Liver
13	chr6:23308400-23309200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:23308400-23309200	Enhancers	NHEK	skin
15	chr6:23308600-23309200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr6:23308800-23309200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:23308800-23309200	Enhancers	Gastric	stomach
18	chr6:23314600-23314800	Bivalent Enhancer	Aorta	Aorta
19	chr6:23315800-23316600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr6:23315800-23317600	Enhancers	HUVEC	blood vessel
21	chr6:23316000-23316400	Enhancers	Primary T cells from cord blood	blood
22	chr6:23316000-23316600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
23	chr6:23316000-23317000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:23316400-23316600	Enhancers	Fetal Kidney	kidney
25	chr6:23319200-23319400	Enhancers	Fetal Muscle Leg	muscle
26	chr6:23319600-23320200	Enhancers	Psoas Muscle	Psoas
27	chr6:23319800-23320400	Enhancers	Fetal Brain Male	brain
28	chr6:23320000-23320200	Enhancers	Fetal Muscle Leg	muscle
29	chr6:23324800-23326000	Enhancers	Fetal Heart	heart
30	chr6:23325600-23326200	Enhancers	Fetal Muscle Leg	muscle
31	chr6:23333000-23336000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr6:23334800-23335200	Enhancers	Left Ventricle	heart
33	chr6:23336000-23336200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr6:23338000-23340000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr6:23339000-23341600	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr6:23339400-23341200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:23339400-23341200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:23339600-23340000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr6:23339800-23340000	Enhancers	Fetal Heart	heart
40	chr6:23340000-23343800	Weak transcription	Fetal Heart	heart
41	chr6:23340400-23341400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:23343800-23344400	Enhancers	Fetal Heart	heart
43	chr6:23347800-23351800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:23349000-23349200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr6:23349200-23349400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr6:23349200-23350000	Enhancers	Muscle Satellite Cultured Cells	--
47	chr6:23349200-23351200	Enhancers	NHDF-Ad	bronchial
48	chr6:23349400-23350000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:23349400-23350400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr6:23349600-23350000	Enhancers	A549	lung

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