Variant report

Variant	nsv1008290
Chromosome Location	chr3:77895292-78308583
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	chr3:78024819-78024962	HepG2	liver:	n/a	n/a
2	BACH1	chr3:78071653-78071664	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:78237298-78237369	K562	blood:	n/a	n/a
4	BATF	chr3:78127129-78127347	GM12878	blood:	n/a	chr3:78127211-78127222
5	BHLHE40	chr3:78208835-78209008	GM12878	blood:	n/a	n/a
6	BHLHE40	chr3:78226084-78226396	HepG2	liver:	n/a	n/a
7	BRCA1	chr3:78190486-78190761	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr3:78281777-78282047	HepG2	liver:	n/a	n/a
9	CEBPB	chr3:78245938-78246136	IMR90	lung:	n/a	n/a
10	CEBPB	chr3:78238913-78239193	HepG2	liver:	n/a	chr3:78239014-78239027 chr3:78239134-78239147
11	CEBPB	chr3:78104933-78105052	HepG2	liver:	n/a	n/a
12	CEBPB	chr3:78233555-78233825	HepG2	liver:	n/a	chr3:78233682-78233691 chr3:78233680-78233691 chr3:78233682-78233691 chr3:78233682-78233691 chr3:78233682-78233691 chr3:78233681-78233692
13	CEBPB	chr3:78067008-78067287	A549	lung:	n/a	n/a
14	CEBPB	chr3:78161460-78161780	Hela-S3	cervix:	n/a	chr3:78161581-78161592 chr3:78161624-78161637 chr3:78161581-78161590
15	CEBPB	chr3:77962712-77963049	HepG2	liver:	n/a	n/a
16	CEBPB	chr3:78203171-78203230	HepG2	liver:	n/a	chr3:78203213-78203224
17	CEBPB	chr3:78072911-78073120	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr3:77910195-77910414	HepG2	liver:	n/a	chr3:77910285-77910296
19	CEBPB	chr3:78067031-78067287	HepG2	liver:	n/a	n/a
20	CEBPB	chr3:78152450-78152724	IMR90	lung:	n/a	chr3:78152606-78152615 chr3:78152606-78152615
21	CEBPB	chr3:78226069-78226400	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr3:78086631-78086672	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr3:78304524-78305000	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:77950514-77950820	A549	lung:	n/a	chr3:77950663-77950674 chr3:77950623-77950634
25	CEBPB	chr3:78304500-78305062	IMR90	lung:	n/a	n/a
26	CEBPB	chr3:78226107-78226378	IMR90	lung:	n/a	n/a
27	CEBPB	chr3:78233520-78233818	IMR90	lung:	n/a	chr3:78233682-78233691 chr3:78233680-78233691 chr3:78233682-78233691 chr3:78233682-78233691 chr3:78233682-78233691 chr3:78233681-78233692
28	CEBPB	chr3:78135302-78135623	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:78226107-78226335	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr3:77950492-77950745	HepG2	liver:	n/a	chr3:77950663-77950674 chr3:77950623-77950634
31	CEBPB	chr3:78098064-78098406	Hela-S3	cervix:	n/a	chr3:78098309-78098322 chr3:78098262-78098273
32	CEBPB	chr3:78161435-78161749	IMR90	lung:	n/a	chr3:78161581-78161592 chr3:78161624-78161637 chr3:78161581-78161590
33	CEBPB	chr3:78245949-78246088	A549	lung:	n/a	n/a
34	CEBPB	chr3:78077473-78077698	HepG2	liver:	n/a	chr3:78077609-78077620
35	CEBPB	chr3:78152449-78152662	A549	lung:	n/a	chr3:78152606-78152615 chr3:78152606-78152615
36	CEBPB	chr3:77924011-77924215	A549	lung:	n/a	n/a
37	CEBPB	chr3:78304565-78304953	HepG2	liver:	n/a	n/a
38	CEBPB	chr3:78190447-78190817	IMR90	lung:	n/a	n/a
39	CEBPB	chr3:78077501-78077704	H1-hESC	embryonic stem cell:	n/a	chr3:78077609-78077620
40	CEBPB	chr3:78233530-78233802	H1-hESC	embryonic stem cell:	n/a	chr3:78233682-78233691 chr3:78233680-78233691 chr3:78233682-78233691 chr3:78233682-78233691 chr3:78233682-78233691 chr3:78233681-78233692
41	CEBPB	chr3:78099499-78099748	HepG2	liver:	n/a	n/a
42	CEBPB	chr3:78190439-78190821	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr3:77983524-77983610	HepG2	liver:	n/a	chr3:77983590-77983601 chr3:77983592-77983603 chr3:77983590-77983603 chr3:77983592-77983603 chr3:77983590-77983603 chr3:77983590-77983603
44	CEBPB	chr3:77936514-77936705	HepG2	liver:	n/a	chr3:77936644-77936655
45	CEBPB	chr3:78067062-78067274	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:78226095-78226342	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:78304566-78304916	A549	lung:	n/a	n/a
48	CEBPB	chr3:78226006-78226358	HepG2	liver:	n/a	n/a
49	CEBPB	chr3:77967360-77967465	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr3:78016148-78016217	A549	lung:	n/a	chr3:78016187-78016198 chr3:78016186-78016197

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:78084695-78084745	MCF10A-Er-Src	breast:	n/a
2	chr3:78233699-78233749	ovcar-3	ovarian:	n/a
3	chr3:78164711-78164761	NB4	blood:	n/a
4	chr3:78233699-78233749	HL-60	blood:	n/a
5	chr3:78078946-78078996	AG04449	skin:	fetal
6	chr3:78079111-78079161	ovcar-3	ovarian:	n/a
7	chr3:78158525-78158575	SK-N-SH_RA	brain:	n/a
8	chr3:78162085-78162135	HepG2	liver:	n/a
9	chr3:78157630-78157680	BE2_C	brain:	n/a
10	chr3:78158525-78158575	PrEC	prostate:	n/a
11	chr3:78084695-78084745	H1-hESC	embryonic stem cell:	embryo
12	chr3:78079111-78079161	AG10803	skin:	n/a
13	chr3:78079111-78079161	HAEpiC	amniotic membrane:	n/a
14	chr3:78157630-78157680	HUVEC	blood vessel:	n/a
15	chr3:78078946-78078996	HepG2	liver:	n/a
16	chr3:78157752-78157802	T-47D	breast:	n/a
17	chr3:78084695-78084745	MCF-7	breast:	n/a
18	chr3:78157630-78157680	Caco-2	colon:	n/a
19	chr3:78233699-78233749	AG09319	gingival:	n/a
20	chr3:78157630-78157680	LNCaP	prostate:	n/a
21	chr3:78084695-78084745	AG10803	skin:	n/a
22	chr3:78158525-78158575	AG04450	lung:	fetal
23	chr3:78079090-78079140	K562	blood:	n/a
24	chr3:78078946-78078996	NHBE	bronchial:	n/a
25	chr3:78157630-78157680	AG10803	skin:	n/a
26	chr3:78079090-78079140	Hepatocyte	liver:	n/a
27	chr3:78157752-78157802	ECC-1	luminal epithelium:	n/a
28	chr3:78079090-78079140	NH-A	brain:	n/a
29	chr3:78157752-78157802	HRCEpiC	kidney:	n/a
30	chr3:78079111-78079161	PFSK-1	brain:	n/a
31	chr3:78157752-78157802	Hela-S3	cervix:	n/a
32	chr3:78157630-78157680	Hela-S3	cervix:	n/a
33	chr3:78079111-78079161	A549	lung:	n/a
34	chr3:78157630-78157680	SKMC	muscle:	n/a
35	chr3:78164711-78164761	GM19239	blood:	n/a
36	chr3:78162085-78162135	IMR90	lung:	fetal
37	chr3:78084695-78084745	Jurkat	blood:	n/a
38	chr3:78079111-78079161	AG09309	skin:	n/a
39	chr3:78157630-78157680	HCM	heart:	n/a
40	chr3:78164711-78164761	Hepatocyte	liver:	n/a
41	chr3:78157752-78157802	MCF-7	breast:	n/a
42	chr3:78079111-78079161	HEK293	kidney:	embryo
43	chr3:78084695-78084745	SK-N-SH	brain:	n/a
44	chr3:78157630-78157680	ECC-1	luminal epithelium:	n/a
45	chr3:78079111-78079161	SAEC	small airway:	n/a
46	chr3:78164711-78164761	PANC-1	pancreas:	n/a
47	chr3:78162085-78162135	GM12878	blood:	n/a
48	chr3:78079111-78079161	SK-N-SH	brain:	n/a
49	chr3:78157630-78157680	NH-A	brain:	n/a
50	chr3:78079090-78079140	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:77397214..77397793-chr3:78253836..78254486,2	MCF-7	breast:
2	chr3:77872762..77874698-chr3:77899434..77901272,2	MCF-7	breast:
3	chr3:77864350..77865332-chr3:78253776..78254517,3	MCF-7	breast:
4	chr3:78071851..78073704-chr3:78086940..78089858,2	K562	blood:
5	chr3:78060869..78061450-chr3:78695066..78696048,2	K562	blood:
6	chr3:78086431..78088297-chr3:78091475..78092990,2	K562	blood:
7	chr3:78268430..78271192-chr3:78649323..78651997,2	MCF-7	breast:
8	chr3:77992294..77995118-chr3:77997205..78000204,3	MCF-7	breast:
9	chr3:77969749..77971465-chr3:77973661..77975250,2	MCF-7	breast:
10	chr11:36066100..36066873-chr3:78116088..78116588,2	MCF-7	breast:
11	chr3:77992294..77995118-chr3:77997205..78000204,3	MCF-7	breast:
12	chr3:77690317..77691982-chr3:77969350..77971249,2	MCF-7	breast:
13	chr3:78071851..78073704-chr3:78086940..78089858,2	K562	blood:
14	chr3:77969749..77971465-chr3:77973661..77975250,2	MCF-7	breast:
15	chr3:78086431..78088297-chr3:78091475..78092990,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ROBO2-1	chr3:78114558-78114598	XLOC_002713
2	lnc-ROBO2-1	chr3:78108303-78108406	XLOC_002713
3	lnc-ROBO1-5	chr3:77982634-77982732	l_2396_chr3:77978476-77982732_testes
4	lnc-ROBO2-1	chr3:78101914-78102171	XLOC_002713
5	lnc-ROBO2-7	chr3:78164309-78164606	NONHSAT090573
6	lnc-ROBO2-8	chr3:78210849-78211143	NONHSAT090574
7	lnc-ROBO1-5	chr3:77978477-77978762	l_2396_chr3:77978476-77982732_testes
8	lnc-ROBO1-5	chr3:77981227-77981312	l_2396_chr3:77978476-77982732_testes
9	lnc-ROBO2-2	chr3:78141274-78141421	XLOC_002714
10	lnc-ROBO1-1	chr3:78087856-78088061	XLOC_003166
11	lnc-ROBO1-5	chr3:77978769-77979156	l_2396_chr3:77978476-77982732_testes
12	lnc-ROBO1-1	chr3:78091293-78091393	XLOC_003166
13	lnc-ROBO2-2	chr3:78136555-78136789	XLOC_002714
14	lnc-ROBO1-1	chr3:78095844-78095945	XLOC_003166
15	lnc-ROBO2-1	chr3:78114193-78114306	XLOC_002713
16	lnc-ROBO2-2	chr3:78140681-78140851	XLOC_002714

Variant related genes	Relation type
ENSG00000264841	TF binding region
ENSG00000240573	TF binding region
RN7SL647P	TF binding region
ENSG00000244461	TF binding region
RN7SKP61	TF binding region
ENSG00000264841	CpG island
ENSG00000240573	CpG island
RN7SL647P	CpG island
ENSG00000244461	CpG island
RN7SKP61	CpG island
ACVR2B	miRNA target sites

Extended variants
information (count: 7385 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:7385 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114805615	chr3:77899430-77899431	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs528453413	chr3:77899531-77899532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs74583312	chr3:77899532-77899533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182867222	chr3:77899533-77899534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372474539	chr3:77899548-77899549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116254950	chr3:77899555-77899556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12631844	chr3:77903203-77903204	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs533487642	chr3:77903212-77903213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs183440701	chr3:77903220-77903221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs567521440	chr3:77903234-77903235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374754771	chr3:77903253-77903254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11127605	chr3:77903343-77903344	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs535075863	chr3:77903375-77903376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs112845467	chr3:77903403-77903404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs116740928	chr3:77903411-77903412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs34401621	chr3:77903493-77903494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187414834	chr3:77903517-77903518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555821557	chr3:77903529-77903530	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76034583	chr3:77903536-77903537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs34703784	chr3:77903538-77903539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190550345	chr3:77903555-77903556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs139875549	chr3:77903557-77903558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs541617010	chr3:77903601-77903602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs561696088	chr3:77903630-77903631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs141717279	chr3:77903639-77903640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183800170	chr3:77903653-77903654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538748654	chr3:77903666-77903667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540631793	chr3:77903676-77903677	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146244870	chr3:77903692-77903693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs375835760	chr3:77903729-77903730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs187932770	chr3:77903741-77903742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs139368362	chr3:77903809-77903810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs564891937	chr3:77903829-77903830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs547329743	chr3:77903860-77903861	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142683204	chr3:77903884-77903885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567682114	chr3:77903889-77903890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs536635256	chr3:77903900-77903901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs560252825	chr3:77903908-77903909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs550342231	chr3:77903925-77903926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs547203334	chr3:77903948-77903949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs570163992	chr3:77903951-77903952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs192999629	chr3:77903975-77903976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs184117272	chr3:77903985-77903986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572517954	chr3:77904018-77904019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532660644	chr3:77904022-77904023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs535356622	chr3:77904025-77904026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs151022689	chr3:77904051-77904052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs141873605	chr3:77904064-77904065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs573622863	chr3:77904103-77904104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114867583	chr3:77904163-77904164	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:606 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:77899400-77899600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:77903200-77904800	Enhancers	HUVEC	blood vessel
3	chr3:77916400-77916800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:77917600-77918000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:77917600-77918800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:77917600-77918800	Enhancers	HMEC	breast
7	chr3:77917600-77918800	Enhancers	NHEK	skin
8	chr3:77917800-77918400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr3:77937000-77938000	Enhancers	Ovary	ovary
10	chr3:77942200-77942400	Enhancers	Pancreas	Pancrea
11	chr3:77945600-77945800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr3:77945800-77947600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr3:77947400-77947600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr3:77947600-77948000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr3:77947600-77955000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr3:77954200-77955800	Enhancers	HUVEC	blood vessel
17	chr3:77954600-77955200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr3:77954600-77956000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr3:77955000-77955800	Enhancers	NH-A	brain
20	chr3:77955000-77956000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr3:77955000-77956000	Enhancers	HMEC	breast
22	chr3:77955000-77956000	Enhancers	NHEK	skin
23	chr3:77955200-77955800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:77955800-77956000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr3:77956000-77968200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr3:77962400-77963200	Enhancers	Liver	Liver
27	chr3:77965600-77967800	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr3:77966200-77966800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr3:77966400-77967600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr3:77966400-77967600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr3:77966600-77967200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:77966600-77967600	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr3:77966800-77967200	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr3:77967200-77968000	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr3:77967600-77968000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr3:77968000-77968600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
37	chr3:77968000-77968600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
38	chr3:77968200-77968800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr3:77968200-77969800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr3:77968800-77972200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr3:77970800-77971800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
42	chr3:77975600-77976200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:77976600-77981400	Enhancers	Ovary	ovary
44	chr3:77977400-77977800	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr3:77977800-77978000	Enhancers	Fetal Kidney	kidney
46	chr3:77977800-77980600	Weak transcription	Pancreatic Islets	Pancreatic Islet
47	chr3:77978000-77978200	Enhancers	Fetal Stomach	stomach
48	chr3:77978000-77978400	Enhancers	Fetal Lung	lung
49	chr3:77978200-77979400	Weak transcription	Fetal Stomach	stomach
50	chr3:77978400-77979800	Weak transcription	Fetal Lung	lung

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