Variant report

Variant	nsv877553
Chromosome Location	chr3:141732321-141786073
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:804)
CpG islands
(count:366)
Chromatin interactive
region (count:50)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:804 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141747897-141748597	K562	blood:	n/a	n/a
2	ARID3A	chr3:141735922-141736175	K562	blood:	n/a	n/a
3	ARID3A	chr3:141740016-141740343	K562	blood:	n/a	n/a
4	ARID3A	chr3:141741164-141741659	K562	blood:	n/a	n/a
5	ARID3A	chr3:141745272-141745595	K562	blood:	n/a	n/a
6	ARID3A	chr3:141744250-141744556	K562	blood:	n/a	n/a
7	ARID3A	chr3:141746444-141747694	K562	blood:	n/a	chr3:141747189-141747205 chr3:141747188-141747204
8	ARID3A	chr3:141764957-141766278	K562	blood:	n/a	n/a
9	ATF1	chr3:141735776-141736084	K562	blood:	n/a	n/a
10	ATF1	chr3:141765160-141765905	K562	blood:	n/a	n/a
11	ATF1	chr3:141741219-141741530	K562	blood:	n/a	n/a
12	ATF2	chr3:141738599-141738995	GM12878	blood:	n/a	n/a
13	ATF2	chr3:141741158-141741597	GM12878	blood:	n/a	n/a
14	ATF3	chr3:141765113-141765513	K562	blood:	n/a	n/a
15	BACH1	chr3:141744283-141744373	K562	blood:	n/a	n/a
16	BACH1	chr3:141733578-141733643	K562	blood:	n/a	n/a
17	BATF	chr3:141741262-141741489	GM12878	blood:	n/a	n/a
18	BATF	chr3:141738609-141738930	GM12878	blood:	n/a	chr3:141738775-141738786
19	BATF	chr3:141747857-141748258	GM12878	blood:	n/a	n/a
20	BATF	chr3:141738639-141738904	GM12878	blood:	n/a	chr3:141738775-141738786
21	BCLAF1	chr3:141747250-141747705	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:141747331-141748152	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:141764829-141766005	K562	blood:	n/a	n/a
24	BHLHE40	chr3:141746686-141746878	K562	blood:	n/a	n/a
25	BHLHE40	chr3:141741289-141741610	K562	blood:	n/a	n/a
26	BHLHE40	chr3:141747846-141747861	K562	blood:	n/a	n/a
27	CBX3	chr3:141747257-141747778	HCT-116	colon:	n/a	n/a
28	CBX3	chr3:141741159-141741668	K562	blood:	n/a	n/a
29	CBX3	chr3:141754371-141754865	K562	blood:	n/a	n/a
30	CBX3	chr3:141746543-141746981	HCT-116	colon:	n/a	n/a
31	CBX3	chr3:141764881-141765958	K562	blood:	n/a	n/a
32	CBX3	chr3:141747898-141748286	K562	blood:	n/a	n/a
33	CBX3	chr3:141765122-141765498	K562	blood:	n/a	n/a
34	CCNT2	chr3:141741211-141741629	K562	blood:	n/a	chr3:141741410-141741430
35	CCNT2	chr3:141748024-141748269	K562	blood:	n/a	n/a
36	CCNT2	chr3:141765174-141766037	K562	blood:	n/a	chr3:141765396-141765416 chr3:141765789-141765809
37	CCNT2	chr3:141735791-141736203	K562	blood:	n/a	n/a
38	CEBPB	chr3:141741296-141741599	K562	blood:	n/a	n/a
39	CEBPB	chr3:141738801-141739090	K562	blood:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
40	CEBPB	chr3:141738846-141739042	A549	lung:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
41	CEBPB	chr3:141738780-141739134	Hela-S3	cervix:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
42	CEBPB	chr3:141784283-141784550	K562	blood:	n/a	n/a
43	CEBPB	chr3:141765132-141765508	K562	blood:	n/a	n/a
44	CEBPB	chr3:141765167-141765981	K562	blood:	n/a	n/a
45	CEBPB	chr3:141741155-141741617	K562	blood:	n/a	n/a
46	CEBPB	chr3:141753473-141753678	K562	blood:	n/a	n/a
47	CEBPB	chr3:141784236-141784580	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr3:141738808-141739134	IMR90	lung:	n/a	chr3:141738950-141738963 chr3:141738932-141738943
49	CEBPB	chr3:141764863-141766102	K562	blood:	n/a	n/a
50	CEBPB	chr3:141784231-141784528	K562	blood:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141764977-141765027	HL-60	blood:	n/a
2	chr3:141764977-141765027	PFSK-1	brain:	n/a
3	chr3:141762963-141763013	HRCEpiC	kidney:	n/a
4	chr3:141764977-141765027	HCF	heart:	n/a
5	chr3:141762963-141763013	ECC-1	luminal epithelium:	n/a
6	chr3:141762780-141762830	MCF10A-Er-Src	breast:	n/a
7	chr3:141764977-141765027	SAEC	small airway:	n/a
8	chr3:141762963-141763013	Caco-2	colon:	n/a
9	chr3:141783929-141783979	HRCEpiC	kidney:	n/a
10	chr3:141762828-141762878	K562	blood:	n/a
11	chr3:141762828-141762878	NHDF-neo	bronchial:	n/a
12	chr3:141783929-141783979	HMEC	breast:	n/a
13	chr3:141762780-141762830	NHBE	bronchial:	n/a
14	chr3:141783929-141783979	NB4	blood:	n/a
15	chr3:141762828-141762878	HRCEpiC	kidney:	n/a
16	chr3:141762963-141763013	HMEC	breast:	n/a
17	chr3:141783929-141783979	MCF10A-Er-Src	breast:	n/a
18	chr3:141783929-141783979	SAEC	small airway:	n/a
19	chr3:141762963-141763013	HEK293	kidney:	embryo
20	chr3:141764977-141765027	AoSMC	blood vessel:	n/a
21	chr3:141748862-141748912	Hepatocyte	liver:	n/a
22	chr3:141764977-141765027	SKMC	muscle:	n/a
23	chr3:141762963-141763013	AoSMC	blood vessel:	n/a
24	chr3:141783929-141783979	AG10803	skin:	n/a
25	chr3:141762963-141763013	NT2-D1	testis:	n/a
26	chr3:141783929-141783979	HCF	heart:	n/a
27	chr3:141762828-141762878	GM12892	blood:	n/a
28	chr3:141783929-141783979	SKMC	muscle:	n/a
29	chr3:141783929-141783979	BJ	skin:	n/a
30	chr3:141764977-141765027	HAEpiC	amniotic membrane:	n/a
31	chr3:141783929-141783979	GM19239	blood:	n/a
32	chr3:141748862-141748912	MCF-7	breast:	n/a
33	chr3:141762963-141763013	SKMC	muscle:	n/a
34	chr3:141764977-141765027	NHBE	bronchial:	n/a
35	chr3:141748862-141748912	SAEC	small airway:	n/a
36	chr3:141762780-141762830	NHDF-neo	bronchial:	n/a
37	chr3:141764977-141765027	PrEC	prostate:	n/a
38	chr3:141762963-141763013	HUVEC	blood vessel:	n/a
39	chr3:141762780-141762830	AG09309	skin:	n/a
40	chr3:141748862-141748912	ProgFib	skin:	n/a
41	chr3:141748862-141748912	GM12891	blood:	n/a
42	chr3:141783929-141783979	ProgFib	skin:	n/a
43	chr3:141783929-141783979	GM12878	blood:	n/a
44	chr3:141762828-141762878	HIPEpiC	eye:	n/a
45	chr3:141748862-141748912	HAEpiC	amniotic membrane:	n/a
46	chr3:141748862-141748912	HepG2	liver:	n/a
47	chr3:141764977-141765027	GM06990	blood:	n/a
48	chr3:141762780-141762830	LNCaP	prostate:	n/a
49	chr3:141748862-141748912	PFSK-1	brain:	n/a
50	chr3:141762963-141763013	HIPEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:141736074..141738288-chr3:141741449..141743046,2	K562	blood:
2	chr3:141765382..141767176-chr3:141772359..141774549,2	K562	blood:
3	chr3:141765382..141767176-chr3:141772359..141774549,2	K562	blood:
4	chr3:141772397..141774089-chr3:141777472..141780381,2	K562	blood:
5	chr3:141752908..141754951-chr3:141758367..141761126,3	K562	blood:
6	chr3:141724450..141726280-chr3:141745104..141746996,2	K562	blood:
7	chr3:141734018..141736974-chr3:141746098..141749383,3	K562	blood:
8	chr3:141740917..141741877-chr3:141764906..141765846,2	K562	blood:
9	chr3:141751486..141755736-chr3:141759507..141766558,8	K562	blood:
10	chr3:141776813..141779383-chr3:141780587..141782430,2	K562	blood:
11	chr3:141726568..141728875-chr3:141730614..141735743,6	K562	blood:
12	chr3:141732044..141735482-chr3:141738671..141741539,4	MCF-7	breast:
13	chr3:141748723..141752115-chr3:141753472..141758138,4	MCF-7	breast:
14	chr3:141740878..141741732-chr3:141899625..141900228,2	MCF-7	breast:
15	chr3:141747854..141750364-chr3:141771803..141774496,2	MCF-7	breast:
16	chr3:141747548..141749276-chr3:141782334..141784054,2	MCF-7	breast:
17	chr3:141736074..141738288-chr3:141741449..141743046,2	K562	blood:
18	chr3:141750870..141754798-chr3:141761535..141764566,4	K562	blood:
19	chr3:141743469..141745043-chr3:141753876..141755747,2	K562	blood:
20	chr3:141740842..141741377-chr3:141998535..141999516,2	K562	blood:
21	chr3:141151754..141154048-chr3:141748045..141749745,2	K562	blood:
22	chr3:141743220..141745863-chr3:141763714..141765255,2	K562	blood:
23	chr3:141742047..141744583-chr3:141758221..141760066,2	K562	blood:
24	chr3:141743220..141745863-chr3:141763714..141765255,2	K562	blood:
25	chr3:141752908..141754951-chr3:141758367..141761126,3	K562	blood:
26	chr3:141746170..141748544-chr3:141765557..141767704,2	K562	blood:
27	chr3:141745791..141750569-chr3:141753730..141757585,7	K562	blood:
28	chr3:141738796..141742970-chr3:141745258..141748964,7	K562	blood:
29	chr3:141748723..141752115-chr3:141753472..141758138,4	MCF-7	breast:
30	chr3:141746178..141749439-chr3:141764015..141767847,4	K562	blood:
31	chr3:141739963..141741863-chr3:141746607..141749166,2	MCF-7	breast:
32	chr3:141767270..141770576-chr3:141773885..141776587,3	K562	blood:
33	chr3:141765860..141768702-chr3:141834792..141837643,2	K562	blood:
34	chr3:141772397..141774089-chr3:141777472..141780381,2	K562	blood:
35	chr3:141767270..141770576-chr3:141773885..141776587,3	K562	blood:
36	chr3:141596118..141597741-chr3:141743168..141745555,2	K562	blood:
37	chr3:141733456..141735928-chr3:141995928..141997484,2	K562	blood:
38	chr3:141726584..141729404-chr3:141730969..141736139,5	K562	blood:
39	chr3:141743896..141745578-chr3:141745998..141747599,2	MCF-7	breast:
40	chr3:141746024..141748965-chr3:160116774..160118286,2	K562	blood:
41	chr3:141743469..141745043-chr3:141753876..141755747,2	K562	blood:
42	chr3:141740917..141741877-chr3:141764906..141765846,2	K562	blood:
43	chr3:141772328..141774089-chr3:141777712..141780381,2	K562	blood:
44	chr1:202085934..202088826-chr3:141779136..141781977,2	K562	blood:
45	chr3:141732044..141735482-chr3:141738671..141741539,4	MCF-7	breast:
46	chr3:141776813..141779383-chr3:141780587..141782430,2	K562	blood:
47	chr3:141742047..141744583-chr3:141758221..141760066,2	K562	blood:
48	chr3:141772328..141774089-chr3:141777712..141780381,2	K562	blood:
49	chr3:141746397..141747918-chr3:142295641..142297892,2	K562	blood:
50	chr3:141739542..141742444-chr3:142003603..142005533,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000233597	TF binding region
TFDP2	TF binding region
ENSG00000233597	CpG island
TFDP2	CpG island
ENSG00000114126	chromatin interactions
ENSG00000069849	chromatin interactions
ENSG00000113810	chromatin interactions
ENSG00000233597	chromatin interactions
ENSG00000068885	chromatin interactions
ENSG00000175054	chromatin interactions

Extended variants
information (count: 1948 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1948 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11569177	chr3:141732321-141732322	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs202217285	chr3:141732322-141732323	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs540496349	chr3:141732335-141732336	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs565555114	chr3:141732357-141732358	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532895282	chr3:141732358-141732359	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs189227859	chr3:141732405-141732406	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs562833541	chr3:141732506-141732507	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530134832	chr3:141732569-141732570	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149371697	chr3:141732611-141732612	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565277347	chr3:141732613-141732614	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540354738	chr3:141732614-141732615	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35931945	chr3:141732622-141732623	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7637962	chr3:141732645-141732646	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs73232644	chr3:141732653-141732654	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs200716315	chr3:141732694-141732695	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112055020	chr3:141732695-141732696	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139098929	chr3:141732731-141732732	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11569176	chr3:141732766-141732767	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538499895	chr3:141732774-141732775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192419694	chr3:141732808-141732809	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556845811	chr3:141732818-141732819	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568478554	chr3:141732823-141732824	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535865982	chr3:141732832-141732833	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554626247	chr3:141732843-141732844	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs572884427	chr3:141732877-141732878	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540808817	chr3:141732887-141732888	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558931085	chr3:141732915-141732916	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144028353	chr3:141732931-141732932	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544888469	chr3:141732938-141732939	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs78600083	chr3:141732955-141732956	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs574867155	chr3:141732965-141732966	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs541893395	chr3:141732966-141732967	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs183749957	chr3:141732976-141732977	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146459045	chr3:141732981-141732982	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76210781	chr3:141732986-141732987	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541334618	chr3:141733001-141733002	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72990256	chr3:141733043-141733044	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs376935749	chr3:141733049-141733050	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550432000	chr3:141733051-141733052	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs150135507	chr3:141733084-141733085	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536226362	chr3:141733091-141733092	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547914595	chr3:141733134-141733135	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79616332	chr3:141733150-141733151	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369934755	chr3:141733151-141733152	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs529937283	chr3:141733154-141733155	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs189143216	chr3:141733182-141733183	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs558637314	chr3:141733185-141733186	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181595294	chr3:141733201-141733202	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569769506	chr3:141733243-141733244	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs538471483	chr3:141733253-141733254	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
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:989 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141629000-141739200	Weak transcription	Psoas Muscle	Psoas
2	chr3:141671800-141735600	Weak transcription	Aorta	Aorta
3	chr3:141677800-141739000	Weak transcription	Left Ventricle	heart
4	chr3:141678800-141745600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
5	chr3:141682800-141739000	Weak transcription	Pancreas	Pancrea
6	chr3:141682800-141745800	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr3:141682800-141746200	Weak transcription	Primary B cells from peripheral blood	blood
8	chr3:141683800-141746600	Weak transcription	Lung	lung
9	chr3:141698600-141738800	Weak transcription	HSMM	muscle
10	chr3:141706400-141746200	Weak transcription	Fetal Lung	lung
11	chr3:141707200-141734400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr3:141708600-141745200	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr3:141711800-141732400	Weak transcription	Stomach Smooth Muscle	stomach
14	chr3:141716000-141732400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:141716000-141738600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr3:141716000-141745600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr3:141719600-141738600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr3:141719600-141738600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr3:141719600-141739000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr3:141720200-141738000	Weak transcription	Fetal Intestine Large	intestine
21	chr3:141720200-141746600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr3:141720400-141732400	Weak transcription	Fetal Stomach	stomach
23	chr3:141720400-141737400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr3:141720400-141742600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr3:141721600-141739000	Weak transcription	Fetal Muscle Leg	muscle
26	chr3:141722600-141735600	Weak transcription	Thymus	Thymus
27	chr3:141722600-141745400	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr3:141723400-141745400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:141723400-141745400	Weak transcription	Fetal Kidney	kidney
30	chr3:141723600-141738400	Weak transcription	Primary B cells from cord blood	blood
31	chr3:141724400-141733000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr3:141724400-141738600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr3:141724400-141741200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:141724400-141745000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr3:141724600-141732400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr3:141724600-141738400	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr3:141724600-141738400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr3:141727200-141732800	Weak transcription	K562	blood
39	chr3:141728200-141746200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
40	chr3:141729400-141736600	Weak transcription	Fetal Intestine Small	intestine
41	chr3:141730400-141734600	Strong transcription	Fetal Thymus	thymus
42	chr3:141731400-141735600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr3:141731400-141738200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr3:141731400-141745400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr3:141731600-141733400	Enhancers	Rectal Smooth Muscle	rectum
46	chr3:141731800-141735600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr3:141732000-141733200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr3:141732000-141733600	Weak transcription	Dnd41	blood
49	chr3:141732200-141732800	Enhancers	Colon Smooth Muscle	Colon
50	chr3:141732200-141733200	Enhancers	Adipose Nuclei	Adipose

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