Variant report

Variant	esv3333253
Chromosome Location	chr3:141585303-141602936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1072)
CpG islands
(count:793)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1072 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141595510-141595632	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:141596764-141597446	K562	blood:	n/a	chr3:141597131-141597147
3	ARID3A	chr3:141594297-141594676	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:141596333-141596464	K562	blood:	n/a	n/a
5	ATF1	chr3:141594386-141595100	K562	blood:	n/a	chr3:141594894-141594908
6	ATF2	chr3:141594300-141594857	GM12878	blood:	n/a	n/a
7	ATF2	chr3:141595381-141595748	GM12878	blood:	n/a	n/a
8	ATF2	chr3:141595404-141595717	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr3:141594340-141594761	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:141596781-141596859	K562	blood:	n/a	n/a
11	BCL3	chr3:141595346-141595694	GM12878	blood:	n/a	chr3:141595421-141595434 chr3:141595550-141595563 chr3:141595558-141595571 chr3:141595604-141595617
12	BCL3	chr3:141594338-141594892	A549	lung:	n/a	n/a
13	BCLAF1	chr3:141594284-141594797	GM12878	blood:	n/a	n/a
14	BCLAF1	chr3:141595412-141595751	GM12878	blood:	n/a	chr3:141595421-141595434 chr3:141595550-141595563 chr3:141595558-141595571 chr3:141595604-141595617
15	BCLAF1	chr3:141595244-141596083	GM12878	blood:	n/a	chr3:141595421-141595434 chr3:141595550-141595563 chr3:141595558-141595571 chr3:141595883-141595892 chr3:141595878-141595891 chr3:141595881-141595894 chr3:141595604-141595617 chr3:141595886-141595895
16	BCLAF1	chr3:141594278-141594708	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:141595371-141596427	HepG2	liver:	n/a	chr3:141595604-141595620 chr3:141595582-141595598 chr3:141595929-141595945
18	BHLHE40	chr3:141595930-141596199	A549	lung:	n/a	n/a
19	BHLHE40	chr3:141594393-141594744	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:141594405-141595149	K562	blood:	n/a	chr3:141595111-141595127
21	BHLHE40	chr3:141595417-141596401	K562	blood:	n/a	chr3:141595604-141595620 chr3:141595582-141595598 chr3:141595929-141595945
22	BHLHE40	chr3:141595074-141596555	GM12878	blood:	n/a	chr3:141595604-141595620 chr3:141595582-141595598 chr3:141595111-141595127 chr3:141595929-141595945
23	BHLHE40	chr3:141594410-141594678	HepG2	liver:	n/a	n/a
24	BHLHE40	chr3:141596862-141596954	K562	blood:	n/a	n/a
25	BRCA1	chr3:141595507-141595687	Hela-S3	cervix:	n/a	n/a
26	BRCA1	chr3:141595152-141595188	HepG2	liver:	n/a	n/a
27	BRCA1	chr3:141595514-141595647	H1-hESC	embryonic stem cell:	n/a	n/a
28	BRCA1	chr3:141594098-141595233	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr3:141593461-141593526	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr3:141594448-141594723	HepG2	liver:	n/a	n/a
31	CBX3	chr3:141594328-141595334	K562	blood:	n/a	n/a
32	CCNT2	chr3:141597214-141597410	K562	blood:	n/a	n/a
33	CCNT2	chr3:141594962-141596344	K562	blood:	n/a	n/a
34	CEBPB	chr3:141597860-141598081	K562	blood:	n/a	n/a
35	CEBPB	chr3:141601001-141601092	H1-hESC	embryonic stem cell:	n/a	chr3:141601038-141601049
36	CEBPB	chr3:141594353-141594689	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr3:141596200-141596398	K562	blood:	n/a	n/a
38	CEBPB	chr3:141597742-141598110	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:141592280-141592488	K562	blood:	n/a	n/a
40	CEBPB	chr3:141594932-141595058	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr3:141600878-141601193	HepG2	liver:	n/a	chr3:141601038-141601049
42	CEBPB	chr3:141597767-141598047	IMR90	lung:	n/a	n/a
43	CEBPB	chr3:141600912-141601168	A549	lung:	n/a	chr3:141601038-141601049
44	CEBPB	chr3:141596716-141597037	IMR90	lung:	n/a	n/a
45	CEBPB	chr3:141595382-141595635	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr3:141600893-141601171	IMR90	lung:	n/a	chr3:141601038-141601049
47	CEBPB	chr3:141600845-141601174	K562	blood:	n/a	chr3:141601038-141601049
48	CEBPD	chr3:141595401-141595797	K562	blood:	n/a	n/a
49	CEBPD	chr3:141595326-141595698	HepG2	liver:	n/a	n/a
50	CEBPD	chr3:141594393-141594605	HepG2	liver:	n/a	n/a

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141596323-141596373	IMR90	lung:	fetal
2	chr3:141595493-141595543	SK-N-MC	brain:	n/a
3	chr3:141596184-141596234	AG10803	skin:	n/a
4	chr3:141595655-141595705	HIPEpiC	eye:	n/a
5	chr3:141594644-141594694	HL-60	blood:	n/a
6	chr3:141599902-141599952	SAEC	small airway:	n/a
7	chr3:141596323-141596373	Hepatocyte	liver:	n/a
8	chr3:141595256-141595306	PrEC	prostate:	n/a
9	chr3:141596184-141596234	SK-N-SH_RA	brain:	n/a
10	chr3:141599902-141599952	GM12892	blood:	n/a
11	chr3:141595655-141595705	HUVEC	blood vessel:	n/a
12	chr3:141595493-141595543	AG10803	skin:	n/a
13	chr3:141595493-141595543	HRE	kidney:	n/a
14	chr3:141595655-141595705	Hepatocyte	liver:	n/a
15	chr3:141595345-141595395	BE2_C	brain:	n/a
16	chr3:141595277-141595327	SK-N-SH	brain:	n/a
17	chr3:141596323-141596373	BE2_C	brain:	n/a
18	chr3:141595345-141595395	NHDF-neo	bronchial:	n/a
19	chr3:141594644-141594694	GM06990	blood:	n/a
20	chr3:141595493-141595543	ProgFib	skin:	n/a
21	chr3:141596323-141596373	AG09319	gingival:	n/a
22	chr3:141595493-141595543	IMR90	lung:	fetal
23	chr3:141594525-141594575	SK-N-MC	brain:	n/a
24	chr3:141595308-141595358	HCT-116	colon:	n/a
25	chr3:141596184-141596234	HRPEpiC	eye:	n/a
26	chr3:141595655-141595705	AG09319	gingival:	n/a
27	chr3:141596184-141596234	BE2_C	brain:	n/a
28	chr3:141596323-141596373	NHDF-neo	bronchial:	n/a
29	chr3:141596323-141596373	AG04449	skin:	fetal
30	chr3:141595103-141595153	CMK	blood:	n/a
31	chr3:141596323-141596373	HCM	heart:	n/a
32	chr3:141595103-141595153	ECC-1	luminal epithelium:	n/a
33	chr3:141594644-141594694	BE2_C	brain:	n/a
34	chr3:141594525-141594575	GM12878	blood:	n/a
35	chr3:141595655-141595705	GM06990	blood:	n/a
36	chr3:141595256-141595306	HEEpiC	esophagus:	n/a
37	chr3:141595655-141595705	HepG2	liver:	n/a
38	chr3:141594525-141594575	AG04449	skin:	fetal
39	chr3:141599902-141599952	SK-N-MC	brain:	n/a
40	chr3:141592597-141592647	HRE	kidney:	n/a
41	chr3:141592597-141592647	NB4	blood:	n/a
42	chr3:141599902-141599952	NH-A	brain:	n/a
43	chr3:141596323-141596373	LNCaP	prostate:	n/a
44	chr3:141592597-141592647	AG04450	lung:	fetal
45	chr3:141595345-141595395	NT2-D1	testis:	n/a
46	chr3:141595655-141595705	HRE	kidney:	n/a
47	chr3:141595345-141595395	AG04449	skin:	fetal
48	chr3:141595493-141595543	U87	brain:	n/a
49	chr3:141595277-141595327	AG10803	skin:	n/a
50	chr3:141595103-141595153	GM19239	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:141598824..141601201-chr3:141604950..141607021,4	MCF-7	breast:
2	chr3:141581516..141585437-chr3:141593335..141595315,3	K562	blood:
3	chr3:141511387..141514014-chr3:141597034..141598647,2	K562	blood:
4	chr3:141447929..141448848-chr3:141594025..141594528,2	K562	blood:
5	chr3:141456960..141457566-chr3:141595354..141595954,2	K562	blood:
6	chr3:141602037..141604850-chr3:141631827..141633593,2	MCF-7	breast:
7	chr3:141594674..141598943-chr3:141621711..141625603,5	MCF-7	breast:
8	chr12:54674483..54675446-chr3:141595145..141596027,2	Hela-S3	cervix:
9	chr3:141582963..141586740-chr3:141593075..141596909,5	MCF-7	breast:
10	chr3:141456347..141457648-chr3:141594019..141595007,11	MCF-7	breast:
11	chr3:141582861..141585388-chr3:141589396..141592365,2	K562	blood:
12	chr3:141574992..141577884-chr3:141596784..141598377,2	K562	blood:
13	chr1:149223784..149224456-chr3:141595271..141595955,2	Hela-S3	cervix:
14	chr17:29297677..29298316-chr3:141594597..141595457,2	Hela-S3	cervix:
15	chr3:141595410..141595997-chr5:41869285..41870151,2	Hela-S3	cervix:
16	chr1:6662875..6663586-chr3:141595164..141595828,2	HCT-116	colon:
17	chr3:141577279..141579253-chr3:141592734..141594463,2	K562	blood:
18	chr3:141456889..141457572-chr3:141594062..141594939,3	MCF-7	breast:
19	chr3:141594460..141597483-chr3:141621419..141624479,3	K562	blood:
20	chr3:141455463..141459614-chr3:141593520..141599146,20	K562	blood:
21	chr3:141581516..141585437-chr3:141593335..141595315,3	K562	blood:
22	chr3:141456324..141457198-chr3:141594736..141595366,2	Hela-S3	cervix:
23	chr3:141452499..141459593-chr3:141591792..141599045,17	MCF-7	breast:
24	chr3:141578632..141580222-chr3:141585498..141587942,2	K562	blood:
25	chr3:141296186..141298105-chr3:141594416..141596281,2	MCF-7	breast:
26	chr3:141462888..141465330-chr3:141599094..141600858,2	K562	blood:
27	chr3:141592835..141597303-chr3:141629979..141635181,8	MCF-7	breast:
28	chr3:141599371..141601007-chr3:141713848..141716781,2	K562	blood:
29	chr3:141455466..141460652-chr3:141593125..141598625,15	K562	blood:
30	chr3:141573267..141574199-chr3:141594125..141594756,3	MCF-7	breast:
31	chr3:141456656..141457567-chr3:141593967..141595178,5	K562	blood:
32	chr16:31470762..31471597-chr3:141595023..141595997,2	Hela-S3	cervix:
33	chr3:141295275..141295993-chr3:141593960..141594866,2	MCF-7	breast:
34	chr3:141582963..141586740-chr3:141593075..141596909,5	MCF-7	breast:
35	chr3:141471164..141473196-chr3:141598108..141600224,2	K562	blood:
36	chr3:141456610..141459064-chr3:141599182..141601879,3	MCF-7	breast:
37	chr3:141455674..141460093-chr3:141592801..141597430,19	MCF-7	breast:
38	chr1:26758364..26759241-chr3:141595118..141595810,2	HCT-116	colon:
39	chr3:141296069..141298248-chr3:141594604..141596170,2	K562	blood:
40	chr3:141584573..141592119-chr3:141592759..141599123,14	K562	blood:
41	chr3:141593925..141596999-chr3:141621116..141624479,3	K562	blood:
42	chr3:141600431..141600931-chr7:138144718..138145221,2	NB4	blood:
43	chr3:141457377..141459578-chr3:141597906..141599752,2	MCF-7	breast:

No data

Variant related genes	Relation type
HMGN2P25	TF binding region
ATP1B3	TF binding region
HMGN2P25	CpG island
ATP1B3	CpG island
ENSG00000117682	chromatin interactions
ENSG00000181481	chromatin interactions
ENSG00000122779	chromatin interactions
ENSG00000260267	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000140691	chromatin interactions
ENSG00000200389	chromatin interactions
ENSG00000155903	chromatin interactions
ENSG00000162413	chromatin interactions
ENSG00000135486	chromatin interactions
ENSG00000206737	chromatin interactions
ENSG00000114125	chromatin interactions
ENSG00000228398	chromatin interactions
ENSG00000248668	chromatin interactions
ENSG00000069849	chromatin interactions

Extended variants
information (count: 652 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:652 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530146508	chr3:141585330-141585331	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs548375857	chr3:141585393-141585394	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs371535753	chr3:141585426-141585427	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs369227510	chr3:141585463-141585464	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs534308677	chr3:141585474-141585475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79105979	chr3:141585648-141585649	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs558736368	chr3:141585649-141585650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556579675	chr3:141585688-141585689	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs531736654	chr3:141585719-141585720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs55859587	chr3:141585749-141585750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs538889105	chr3:141585758-141585759	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529160595	chr3:141585760-141585761	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554618558	chr3:141585826-141585827	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557268687	chr3:141585857-141585858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs7613481	chr3:141585865-141585866	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs542636064	chr3:141585900-141585901	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs571136757	chr3:141585901-141585902	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs576977191	chr3:141585978-141585979	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs186606465	chr3:141585988-141585989	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191003321	chr3:141585994-141585995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs537740464	chr3:141586075-141586076	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs556468045	chr3:141586162-141586163	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76857146	chr3:141586171-141586172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs181679335	chr3:141586247-141586248	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113249412	chr3:141586254-141586255	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs139994741	chr3:141586304-141586305	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs185959835	chr3:141586354-141586355	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs190577275	chr3:141586361-141586362	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112634551	chr3:141586362-141586363	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576545929	chr3:141586385-141586386	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs150018218	chr3:141586387-141586388	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs527743580	chr3:141586406-141586407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs547128910	chr3:141586409-141586410	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs111714453	chr3:141586430-141586431	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs567030386	chr3:141586443-141586444	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs148782297	chr3:141586462-141586463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs538876248	chr3:141586466-141586467	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545513618	chr3:141586521-141586522	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs536295955	chr3:141586523-141586524	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556953818	chr3:141586525-141586526	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs569105442	chr3:141586565-141586566	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs142453763	chr3:141586583-141586584	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs554511361	chr3:141586608-141586609	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs13076831	chr3:141586610-141586611	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs377542203	chr3:141586614-141586615	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs397875017	chr3:141586710-141586711	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs539938535	chr3:141586721-141586722	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558273300	chr3:141586726-141586727	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs555906385	chr3:141586733-141586734	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577004796	chr3:141586735-141586736	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:777 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141580800-141588600	Weak transcription	HUVEC	blood vessel
2	chr3:141581800-141585400	Weak transcription	K562	blood
3	chr3:141583800-141588800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:141585200-141585400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:141585400-141585600	Enhancers	HSMMtube	muscle
6	chr3:141585400-141585600	Enhancers	K562	blood
7	chr3:141585600-141588600	Weak transcription	HSMMtube	muscle
8	chr3:141588200-141588600	Enhancers	Fetal Muscle Trunk	muscle
9	chr3:141588600-141589600	Enhancers	HSMMtube	muscle
10	chr3:141588600-141589600	Enhancers	HUVEC	blood vessel
11	chr3:141588600-141593800	Weak transcription	Fetal Muscle Trunk	muscle
12	chr3:141588800-141589200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr3:141589000-141589600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr3:141589000-141589600	Enhancers	HMEC	breast
15	chr3:141589000-141589800	Enhancers	NHEK	skin
16	chr3:141589200-141593400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr3:141589600-141593400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr3:141589600-141593400	Weak transcription	HMEC	breast
19	chr3:141589600-141593400	Weak transcription	HUVEC	blood vessel
20	chr3:141589600-141593800	Weak transcription	HSMMtube	muscle
21	chr3:141589800-141593400	Weak transcription	NHEK	skin
22	chr3:141593200-141593400	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr3:141593400-141593600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
24	chr3:141593400-141593800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr3:141593400-141593800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr3:141593400-141593800	Enhancers	Fetal Brain Male	brain
27	chr3:141593400-141593800	Enhancers	Dnd41	blood
28	chr3:141593400-141594000	Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr3:141593400-141594000	Active TSS	iPS-18 Cell Line	embryonic stem cell
30	chr3:141593400-141594000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr3:141593400-141594000	Active TSS	Muscle Satellite Cultured Cells	--
32	chr3:141593400-141594000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr3:141593400-141594000	Active TSS	Duodenum Mucosa	Duodenum
34	chr3:141593400-141594000	Active TSS	A549	lung
35	chr3:141593400-141594000	Active TSS	NHEK	skin
36	chr3:141593400-141594200	Enhancers	HUVEC	blood vessel
37	chr3:141593400-141594400	Enhancers	Primary T killer memory cells from peripheral blood	blood
38	chr3:141593400-141594400	Enhancers	Fetal Intestine Small	intestine
39	chr3:141593400-141594800	Active TSS	HepG2	liver
40	chr3:141593400-141595000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr3:141593400-141596600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr3:141593400-141597400	Active TSS	iPS-15b Cell Line	embryonic stem cell
43	chr3:141593400-141597600	Active TSS	Fetal Kidney	kidney
44	chr3:141593400-141597600	Active TSS	HMEC	breast
45	chr3:141593400-141597600	Active TSS	NHLF	lung
46	chr3:141593400-141598000	Active TSS	ES-I3 Cell Line	embryonic stem cell
47	chr3:141593600-141593800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr3:141593600-141593800	Enhancers	Adipose Nuclei	Adipose
49	chr3:141593600-141593800	Enhancers	Rectal Mucosa Donor 29	rectum
50	chr3:141593600-141593800	Enhancers	Hela-S3	cervix

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