Variant report

Variant	nsv591925
Chromosome Location	chr3:143821997-144019763
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:741)
CpG islands
(count:183)
Chromatin interactive
region (count:51)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143837779-143837958	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:143880755-143881509	HepG2	liver:	n/a	chr3:143881380-143881396
3	ATF1	chr3:143825901-143826204	K562	blood:	n/a	n/a
4	ATF2	chr3:143848478-143849143	GM12878	blood:	n/a	n/a
5	ATF2	chr3:144013376-144014503	GM12878	blood:	n/a	n/a
6	ATF2	chr3:143846465-143847491	GM12878	blood:	n/a	n/a
7	ATF2	chr3:143848494-143849137	GM12878	blood:	n/a	n/a
8	ATF2	chr3:144013394-144014434	GM12878	blood:	n/a	n/a
9	ATF2	chr3:143846788-143847440	GM12878	blood:	n/a	n/a
10	BACH1	chr3:143833588-143833943	K562	blood:	n/a	chr3:143833761-143833775
11	BACH1	chr3:143833582-143834019	H1-hESC	embryonic stem cell:	n/a	chr3:143833761-143833775
12	BATF	chr3:144013492-144013785	GM12878	blood:	n/a	n/a
13	BATF	chr3:143846881-143847436	GM12878	blood:	n/a	n/a
14	BATF	chr3:144013981-144014356	GM12878	blood:	n/a	n/a
15	BATF	chr3:144013966-144014424	GM12878	blood:	n/a	n/a
16	BATF	chr3:143848423-143849121	GM12878	blood:	n/a	n/a
17	BATF	chr3:144007957-144008191	GM12878	blood:	n/a	n/a
18	BATF	chr3:143828841-143829119	GM12878	blood:	n/a	n/a
19	BATF	chr3:144015695-144015975	GM12878	blood:	n/a	n/a
20	BATF	chr3:143848617-143849040	GM12878	blood:	n/a	n/a
21	BATF	chr3:144013488-144013758	GM12878	blood:	n/a	n/a
22	BATF	chr3:144015688-144015947	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:143848674-143849066	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:144013972-144014361	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:144014007-144014300	GM12878	blood:	n/a	n/a
26	BCL11A	chr3:144013477-144013896	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:143848485-143849120	GM12878	blood:	n/a	n/a
28	BCL11A	chr3:144013523-144013694	GM12878	blood:	n/a	n/a
29	BCL11A	chr3:144015708-144016008	GM12878	blood:	n/a	n/a
30	BCL3	chr3:144013975-144014412	GM12878	blood:	n/a	n/a
31	BCL3	chr3:144013510-144013878	GM12878	blood:	n/a	n/a
32	BCL3	chr3:143848594-143849036	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:144013925-144014474	GM12878	blood:	n/a	n/a
34	BCLAF1	chr3:144013490-144013836	GM12878	blood:	n/a	n/a
35	BCLAF1	chr3:143846960-143847480	GM12878	blood:	n/a	n/a
36	BCLAF1	chr3:144013974-144014372	GM12878	blood:	n/a	n/a
37	BCLAF1	chr3:143846949-143847398	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:143825952-143826076	K562	blood:	n/a	n/a
39	BHLHE40	chr3:143828859-143828869	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:144014030-144014341	GM12878	blood:	n/a	n/a
41	CCNT2	chr3:143881095-143881198	K562	blood:	n/a	n/a
42	CEBPB	chr3:143837707-143838082	IMR90	lung:	n/a	chr3:143837889-143837900
43	CEBPB	chr3:143906442-143906770	A549	lung:	n/a	chr3:143906601-143906612 chr3:143906603-143906612
44	CEBPB	chr3:143897455-143897752	K562	blood:	n/a	chr3:143897627-143897636 chr3:143897626-143897637 chr3:143897627-143897636 chr3:143897627-143897636
45	CEBPB	chr3:143897454-143897839	ECC-1	luminal epithelium:	n/a	chr3:143897627-143897636 chr3:143897626-143897637 chr3:143897627-143897636 chr3:143897627-143897636
46	CEBPB	chr3:143837747-143837971	Hela-S3	cervix:	n/a	chr3:143837889-143837900
47	CEBPB	chr3:143831383-143831625	HepG2	liver:	n/a	chr3:143831545-143831558 chr3:143831545-143831556
48	CEBPB	chr3:143978456-143978653	A549	lung:	n/a	n/a
49	CEBPB	chr3:143992939-143993236	IMR90	lung:	n/a	chr3:143993110-143993121
50	CEBPB	chr3:143897551-143897790	A549	lung:	n/a	chr3:143897627-143897636 chr3:143897626-143897637 chr3:143897627-143897636 chr3:143897627-143897636

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143993048-143993098	H1-hESC	embryonic stem cell:	embryo
2	chr3:143847318-143847368	GM12892	blood:	n/a
3	chr3:143847318-143847368	NT2-D1	testis:	n/a
4	chr3:143993048-143993098	GM12891	blood:	n/a
5	chr3:143847318-143847368	NH-A	brain:	n/a
6	chr3:143847318-143847368	HRCEpiC	kidney:	n/a
7	chr3:143993048-143993098	AG04450	lung:	fetal
8	chr3:143847318-143847368	AG09309	skin:	n/a
9	chr3:143993048-143993098	RPTEC	kidney:	n/a
10	chr3:143847318-143847368	HPAEpiC	pulmonary alveolar:	n/a
11	chr3:143847318-143847368	HEK293	kidney:	embryo
12	chr3:143847318-143847368	HAEpiC	amniotic membrane:	n/a
13	chr3:143861209-143861259	SAEC	small airway:	n/a
14	chr3:143993048-143993098	Jurkat	blood:	n/a
15	chr3:143847318-143847368	HCT-116	colon:	n/a
16	chr3:143861209-143861259	HCM	heart:	n/a
17	chr3:143993048-143993098	HCM	heart:	n/a
18	chr3:143861209-143861259	CMK	blood:	n/a
19	chr3:143847318-143847368	HNPCEpiC	eye:	n/a
20	chr3:143993048-143993098	HCF	heart:	n/a
21	chr3:143861209-143861259	NHDF-neo	bronchial:	n/a
22	chr3:143993048-143993098	U87	brain:	n/a
23	chr3:143861209-143861259	T-47D	breast:	n/a
24	chr3:143861209-143861259	HIPEpiC	eye:	n/a
25	chr3:143847318-143847368	ProgFib	skin:	n/a
26	chr3:143847318-143847368	SK-N-MC	brain:	n/a
27	chr3:143993048-143993098	AG04449	skin:	fetal
28	chr3:143847318-143847368	HCM	heart:	n/a
29	chr3:143993048-143993098	Hela-S3	cervix:	n/a
30	chr3:143993048-143993098	HNPCEpiC	eye:	n/a
31	chr3:143993048-143993098	HAEpiC	amniotic membrane:	n/a
32	chr3:143847318-143847368	Jurkat	blood:	n/a
33	chr3:143847318-143847368	MCF-7	breast:	n/a
34	chr3:143847318-143847368	NHDF-neo	bronchial:	n/a
35	chr3:143861209-143861259	HL-60	blood:	n/a
36	chr3:143861209-143861259	HCT-116	colon:	n/a
37	chr3:143861209-143861259	Hepatocyte	liver:	n/a
38	chr3:143847318-143847368	GM12878	blood:	n/a
39	chr3:143861209-143861259	AG09319	gingival:	n/a
40	chr3:143861209-143861259	BE2_C	brain:	n/a
41	chr3:143847318-143847368	Caco-2	colon:	n/a
42	chr3:143993048-143993098	BE2_C	brain:	n/a
43	chr3:143861209-143861259	Caco-2	colon:	n/a
44	chr3:143847318-143847368	ovcar-3	ovarian:	n/a
45	chr3:143993048-143993098	AG10803	skin:	n/a
46	chr3:143861209-143861259	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:143993048-143993098	A549	lung:	n/a
48	chr3:143993048-143993098	PrEC	prostate:	n/a
49	chr3:143847318-143847368	AG09319	gingival:	n/a
50	chr3:143993048-143993098	HRE	kidney:	n/a

(count:51 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:143690547..143692210-chr3:143990164..143992308,2	MCF-7	breast:
2	chr3:143892804..143894519-chr3:143897127..143900073,2	K562	blood:
3	chr3:143849261..143851661-chr3:143853910..143857233,3	K562	blood:
4	chr3:144012906..144014762-chr3:144016607..144019319,2	MCF-7	breast:
5	chr3:143872336..143874000-chr3:143882246..143884179,2	K562	blood:
6	chr3:143852522..143855348-chr3:143858842..143861138,3	K562	blood:
7	chr3:143900814..143902970-chr3:143905127..143907243,2	K562	blood:
8	chr3:143976073..143978906-chr3:143983000..143985910,2	K562	blood:
9	chr3:143970717..143972446-chr3:143972808..143975131,2	K562	blood:
10	chr3:143985749..143987878-chr3:143995682..143998153,2	MCF-7	breast:
11	chr3:143852522..143854486-chr3:143858842..143860873,2	K562	blood:
12	chr3:143940644..143942210-chr3:144039456..144041845,2	MCF-7	breast:
13	chr3:143852522..143854486-chr3:143858842..143860873,2	K562	blood:
14	chr12:53061288..53061963-chr3:143990811..143991640,2	MCF-7	breast:
15	chr3:143693440..143695168-chr3:143824981..143826507,2	K562	blood:
16	chr3:143976073..143978906-chr3:143983000..143985910,2	K562	blood:
17	chr3:143691791..143694005-chr3:143990028..143992353,2	K562	blood:
18	chr3:143690019..143692645-chr3:143838592..143840602,2	MCF-7	breast:
19	chr3:143690098..143692740-chr3:143921809..143923787,2	MCF-7	breast:
20	chr3:143890771..143894320-chr3:143898037..143901332,4	MCF-7	breast:
21	chr3:143862145..143864475-chr3:143867360..143869304,2	K562	blood:
22	chr3:143851188..143852094-chr3:143864087..143864848,2	MCF-7	breast:
23	chr3:143962916..143965594-chr3:143970666..143973506,3	MCF-7	breast:
24	chr3:143819810..143821704-chr3:143822907..143824829,2	K562	blood:
25	chr3:143690687..143692253-chr3:144007125..144008743,2	MCF-7	breast:
26	chr3:143890771..143894320-chr3:143898037..143901332,4	MCF-7	breast:
27	chr3:143849261..143851661-chr3:143853910..143857233,3	K562	blood:
28	chr3:143886285..143888723-chr3:143892668..143894323,2	MCF-7	breast:
29	chr3:143690118..143691701-chr3:143832544..143834145,2	K562	blood:
30	chr3:61879348..61880969-chr3:143831622..143834006,2	MCF-7	breast:
31	chr3:143865202..143867000-chr3:143870211..143871810,2	K562	blood:
32	chr3:143902901..143904761-chr3:143930558..143932653,2	MCF-7	breast:
33	chr19:18990145..18992533-chr3:143946835..143949727,2	MCF-7	breast:
34	chr3:143882905..143885862-chr3:143887105..143889283,2	MCF-7	breast:
35	chr3:143882905..143885862-chr3:143887105..143889283,2	MCF-7	breast:
36	chr3:143892804..143894519-chr3:143897127..143900073,2	K562	blood:
37	chr3:143962916..143965594-chr3:143970666..143973506,3	MCF-7	breast:
38	chr3:143985749..143987878-chr3:143995682..143998153,2	MCF-7	breast:
39	chr3:143862145..143864475-chr3:143867360..143869304,2	K562	blood:
40	chr3:143865202..143867000-chr3:143870211..143871810,2	K562	blood:
41	chr3:143872336..143874000-chr3:143882246..143884179,2	K562	blood:
42	chr3:143690008..143692264-chr3:143879594..143881502,2	MCF-7	breast:
43	chr3:143892267..143895225-chr3:144092173..144094543,2	MCF-7	breast:
44	chr3:143694158..143694846-chr3:143996996..143997942,2	MCF-7	breast:
45	chr3:143689793..143693071-chr3:143879753..143882837,6	MCF-7	breast:
46	chr3:143886285..143888723-chr3:143892668..143894323,2	MCF-7	breast:
47	chr3:143902901..143904761-chr3:143930558..143932653,2	MCF-7	breast:
48	chr3:143851188..143852094-chr3:143864087..143864848,2	MCF-7	breast:
49	chr3:144012906..144014762-chr3:144016607..144019319,2	MCF-7	breast:
50	chr3:143852522..143855348-chr3:143858842..143861138,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf58-1	chr3:143936262-143938475	NONHSAT092535

No data

Variant related genes	Relation type
RNA5SP144	TF binding region
RNA5SP144	CpG island
ENSG00000181744	chromatin interactions
ENSG00000222778	chromatin interactions
ENSG00000269694	chromatin interactions

Extended variants
information (count: 5389 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:5389 , 50 per page) page: 1 2 3 4 5 6 7 ... 108

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6781063	chr3:143821997-143821998	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532967112	chr3:143822039-143822040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs79899531	chr3:143822052-143822053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs80093199	chr3:143822053-143822054	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540339357	chr3:143822098-143822099	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148632761	chr3:143822179-143822180	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs530766261	chr3:143822192-143822193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs549073045	chr3:143822204-143822205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561035837	chr3:143822272-143822273	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs528728036	chr3:143822302-143822303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs546857246	chr3:143822331-143822332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9821065	chr3:143822362-143822363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571941884	chr3:143822412-143822413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538977862	chr3:143822425-143822426	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374318241	chr3:143822428-143822429	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs368427189	chr3:143822473-143822474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551267043	chr3:143822496-143822497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs376991806	chr3:143822541-143822542	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs370346734	chr3:143822579-143822580	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536957695	chr3:143822608-143822609	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568874437	chr3:143822637-143822638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs115438836	chr3:143822742-143822743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs373045410	chr3:143822762-143822763	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs554745828	chr3:143822783-143822784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs572972421	chr3:143822974-143822975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560649213	chr3:143823042-143823043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs371269437	chr3:143823078-143823079	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs190997661	chr3:143823084-143823085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558458987	chr3:143823102-143823103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375078909	chr3:143823117-143823118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs62269932	chr3:143823129-143823130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs544179879	chr3:143823176-143823177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567220384	chr3:143823216-143823217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs555997498	chr3:143823217-143823218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs534725655	chr3:143823230-143823231	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529012834	chr3:143823255-143823256	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34353207	chr3:143823296-143823297	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376595338	chr3:143823342-143823343	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs9809059	chr3:143823401-143823402	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372055574	chr3:143823467-143823468	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578045403	chr3:143823555-143823556	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs548768422	chr3:143823559-143823560	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs142186006	chr3:143823610-143823611	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs151187385	chr3:143823659-143823660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540687013	chr3:143823701-143823702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545455247	chr3:143823718-143823719	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565357804	chr3:143823726-143823727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12488383	chr3:143823750-143823751	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140403436	chr3:143823751-143823752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs569562970	chr3:143823768-143823769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
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
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
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Breast cancer	21509527	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143818600-143824000	Weak transcription	Ovary	ovary
2	chr3:143819000-143823000	Weak transcription	Liver	Liver
3	chr3:143819200-143823000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:143819200-143823000	Weak transcription	Aorta	Aorta
5	chr3:143819200-143824400	Weak transcription	Pancreas	Pancrea
6	chr3:143820800-143822000	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr3:143821000-143822000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:143821000-143822000	Enhancers	Duodenum Smooth Muscle	Duodenum
9	chr3:143821000-143822200	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr3:143821000-143822400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr3:143821000-143822400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr3:143821200-143822000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr3:143821200-143822000	Enhancers	Stomach Smooth Muscle	stomach
14	chr3:143821200-143822400	Enhancers	H1 Cell Line	embryonic stem cell
15	chr3:143821200-143824600	Enhancers	Cortex derived primary cultured neurospheres	brain
16	chr3:143821200-143824800	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr3:143821400-143822400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr3:143821400-143823600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr3:143821400-143828800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr3:143821600-143822800	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr3:143821600-143823000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr3:143821600-143823800	Enhancers	Brain Germinal Matrix	brain
23	chr3:143821600-143824600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:143821800-143822200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr3:143821800-143829000	Weak transcription	Brain Hippocampus Middle	brain
26	chr3:143822000-143823000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr3:143822000-143823200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr3:143822200-143823400	Enhancers	Fetal Muscle Leg	muscle
29	chr3:143822400-143823800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:143822400-143824000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:143822400-143824600	Enhancers	Brain Anterior Caudate	brain
32	chr3:143823000-143823200	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr3:143823000-143823200	Enhancers	H9 Cell Line	embryonic stem cell
34	chr3:143823000-143823200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr3:143823000-143823400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr3:143823000-143823400	Enhancers	Aorta	Aorta
37	chr3:143823000-143823800	Enhancers	Adipose Nuclei	Adipose
38	chr3:143823000-143825000	Enhancers	Liver	Liver
39	chr3:143823200-143823400	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr3:143823200-143823800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:143823200-143823800	Enhancers	Psoas Muscle	Psoas
42	chr3:143823200-143824000	Enhancers	Duodenum Smooth Muscle	Duodenum
43	chr3:143823600-143823800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr3:143823800-143824200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr3:143824200-143825000	Enhancers	HepG2	liver
46	chr3:143824200-143825200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:143824400-143824600	Enhancers	Ovary	ovary
48	chr3:143824400-143825200	Enhancers	Pancreas	Pancrea
49	chr3:143824600-143828800	Weak transcription	Brain Anterior Caudate	brain
50	chr3:143824600-143829600	Weak transcription	Cortex derived primary cultured neurospheres	brain

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