Variant report

Variant	nsv1004944
Chromosome Location	chr3:163968837-164110498
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	BHLHE40	chr3:164065590-164065659	K562	blood:	n/a	n/a
2	CEBPB	chr3:164077996-164078260	A549	lung:	n/a	chr3:164078134-164078145
3	CEBPB	chr3:164107093-164107343	IMR90	lung:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
4	CEBPB	chr3:164077987-164078333	Hela-S3	cervix:	n/a	chr3:164078134-164078145
5	CEBPB	chr3:164085628-164085750	K562	blood:	n/a	n/a
6	CEBPB	chr3:164097994-164098357	MCF-7	breast:	n/a	n/a
7	CEBPB	chr3:164093357-164093663	A549	lung:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
8	CEBPB	chr3:164107072-164107346	HepG2	liver:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
9	CEBPB	chr3:163980067-163980373	HepG2	liver:	n/a	chr3:163980184-163980195
10	CEBPB	chr3:164078064-164078196	HepG2	liver:	n/a	chr3:164078134-164078145
11	CEBPB	chr3:164093320-164093640	HepG2	liver:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
12	CEBPB	chr3:164078081-164078324	MCF-7	breast:	n/a	chr3:164078134-164078145
13	CEBPB	chr3:163980107-163980307	H1-hESC	embryonic stem cell:	n/a	chr3:163980184-163980195
14	CEBPB	chr3:164066095-164066166	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr3:164078036-164078173	H1-hESC	embryonic stem cell:	n/a	chr3:164078134-164078145
16	CEBPB	chr3:164107081-164107356	A549	lung:	n/a	chr3:164107227-164107236 chr3:164107225-164107238 chr3:164107227-164107236 chr3:164107227-164107236 chr3:164107226-164107237 chr3:164107225-164107238 chr3:164107225-164107236 chr3:164107227-164107236
17	CEBPB	chr3:164093408-164093523	K562	blood:	n/a	chr3:164093476-164093487
18	CEBPB	chr3:163980083-163980289	Hela-S3	cervix:	n/a	chr3:163980184-163980195
19	CEBPB	chr3:164093370-164093659	Hela-S3	cervix:	n/a	chr3:164093476-164093487 chr3:164093572-164093583
20	CEBPB	chr3:163980076-163980312	A549	lung:	n/a	chr3:163980184-163980195
21	CEBPB	chr3:164077961-164078328	HepG2	liver:	n/a	chr3:164078134-164078145
22	CEBPB	chr3:164085608-164085831	IMR90	lung:	n/a	chr3:164085753-164085766
23	CTBP2	chr3:164038799-164039115	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr3:164107980-164108130	AoAF	blood vessel:	n/a	n/a
25	CTCF	chr3:164094140-164094290	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:164108000-164108150	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:164093925-164094062	HepG2	liver:	n/a	n/a
28	CTCF	chr3:164107980-164108130	HL-60	blood:	n/a	n/a
29	CTCF	chr3:163979232-163979359	K562	blood:	n/a	n/a
30	CTCF	chr3:164050680-164050830	WERI-Rb-1	eye:	n/a	n/a
31	CTCF	chr3:164107960-164108110	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr3:164107980-164108130	GM12878	blood:	n/a	n/a
33	CTCF	chr3:164093834-164094142	GM12878	blood:	n/a	n/a
34	CTCF	chr3:164107980-164108130	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr3:163968800-163968950	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
36	CTCF	chr3:164107980-164108130	HCFaa	heart:	n/a	n/a
37	CTCF	chr3:163968785-163969078	MCF-7	breast:	n/a	chr3:163968895-163968916 chr3:163968905-163968913 chr3:163968901-163968917
38	CTCF	chr3:164107600-164107750	HRE	kidney:	n/a	n/a
39	CTCF	chr3:164108060-164108210	HCT-116	colon:	n/a	n/a
40	CTCF	chr3:164050760-164050812	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:164108020-164108170	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr3:164093900-164094050	AG09319	gingival:	n/a	n/a
43	CTCF	chr3:164108000-164108150	GM12867	blood:	n/a	n/a
44	CTCF	chr3:164108100-164108250	HCT-116	colon:	n/a	n/a
45	CTCF	chr3:164093914-164094075	Medullo	brain:	n/a	n/a
46	CTCF	chr3:164093860-164094010	RPTEC	kidney:	n/a	n/a
47	CTCF	chr3:164108059-164108118	GM13977	blood:	n/a	n/a
48	CTCF	chr3:164093900-164094050	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr3:164107920-164108070	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr3:164050700-164050850	HAc	cerebellar:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:164059255-164059305	NHBE	bronchial:	n/a
2	chr3:164059255-164059305	NHBE	bronchial:	n/a
3	chr3:164056753-164056803	Hela-S3	cervix:	n/a
4	chr3:164059255-164059305	AG04449	skin:	fetal
5	chr3:164050953-164051003	Hela-S3	cervix:	n/a
6	chr3:164056753-164056803	HCF	heart:	n/a
7	chr3:164059011-164059061	AG10803	skin:	n/a
8	chr3:164059011-164059061	SK-N-SH	brain:	n/a
9	chr3:164056753-164056803	AG10803	skin:	n/a
10	chr3:164059255-164059305	HRE	kidney:	n/a
11	chr3:164009569-164009619	HNPCEpiC	eye:	n/a
12	chr3:164056753-164056803	MCF10A-Er-Src	breast:	n/a
13	chr3:164059124-164059174	CMK	blood:	n/a
14	chr3:164009569-164009619	A549	lung:	n/a
15	chr3:164056753-164056803	HRCEpiC	kidney:	n/a
16	chr3:164059011-164059061	HL-60	blood:	n/a
17	chr3:164050953-164051003	NH-A	brain:	n/a
18	chr3:164009569-164009619	HMEC	breast:	n/a
19	chr3:164056463-164056513	HRE	kidney:	n/a
20	chr3:164059011-164059061	HCF	heart:	n/a
21	chr3:164056753-164056803	GM19239	blood:	n/a
22	chr3:164059011-164059061	PFSK-1	brain:	n/a
23	chr3:164050953-164051003	Hepatocyte	liver:	n/a
24	chr3:164059255-164059305	HCM	heart:	n/a
25	chr3:164059124-164059174	SK-N-SH	brain:	n/a
26	chr3:164059011-164059061	ECC-1	luminal epithelium:	n/a
27	chr3:164056753-164056803	T-47D	breast:	n/a
28	chr3:164056463-164056513	Caco-2	colon:	n/a
29	chr3:164059124-164059174	HRCEpiC	kidney:	n/a
30	chr3:164050953-164051003	NHBE	bronchial:	n/a
31	chr3:164059011-164059061	MCF-7	breast:	n/a
32	chr3:164056753-164056803	ECC-1	luminal epithelium:	n/a
33	chr3:164059124-164059174	HCPEpiC	choroid plexus:	n/a
34	chr3:164056463-164056513	HepG2	liver:	n/a
35	chr3:164050953-164051003	AG09309	skin:	n/a
36	chr3:164009569-164009619	HIPEpiC	eye:	n/a
37	chr3:164009569-164009619	SK-N-MC	brain:	n/a
38	chr3:164059011-164059061	HRPEpiC	eye:	n/a
39	chr3:164056463-164056513	HL-60	blood:	n/a
40	chr3:164050953-164051003	AG10803	skin:	n/a
41	chr3:164059255-164059305	HIPEpiC	eye:	n/a
42	chr3:164009569-164009619	HCF	heart:	n/a
43	chr3:164059124-164059174	AG09319	gingival:	n/a
44	chr3:164009569-164009619	AG10803	skin:	n/a
45	chr3:164009569-164009619	BE2_C	brain:	n/a
46	chr3:164059124-164059174	AG10803	skin:	n/a
47	chr3:164059255-164059305	NB4	blood:	n/a
48	chr3:164059255-164059305	HCF	heart:	n/a
49	chr3:164050953-164051003	K562	blood:	n/a
50	chr3:164056463-164056513	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
2	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
3	chr3:164097647..164098678-chr3:164154502..164155534,10	MCF-7	breast:
4	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
5	chr3:164050649..164051226-chr3:164523700..164524566,2	MCF-7	breast:
6	chr3:163995585..163997750-chr3:164093655..164096327,2	K562	blood:
7	chr3:164097711..164098324-chr3:164241488..164242187,2	MCF-7	breast:
8	chr3:164033562..164036466-chr3:164041623..164043945,2	MCF-7	breast:
9	chr3:164097659..164099012-chr3:164352282..164353331,34	MCF-7	breast:
10	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
11	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
12	chr3:164097708..164098703-chr3:164352353..164353241,9	MCF-7	breast:
13	chr3:164097711..164099012-chr3:164352332..164353250,14	MCF-7	breast:
14	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
15	chr3:164097731..164098551-chr3:164154660..164155422,4	MCF-7	breast:
16	chr3:163988892..163990964-chr3:163991912..163993953,2	K562	blood:
17	chr3:164072695..164075481-chr3:164078791..164081086,2	MCF-7	breast:
18	chr3:164093244..164094225-chr3:164903325..164904113,2	MCF-7	breast:
19	chr3:164097709..164098424-chr3:164241494..164242452,3	MCF-7	breast:
20	chr3:164032173..164034796-chr3:164095339..164097722,2	K562	blood:
21	chr3:163968485..163970197-chr3:163971709..163973734,2	MCF-7	breast:
22	chr3:164097711..164098324-chr3:164241488..164242482,3	MCF-7	breast:
23	chr3:164097647..164098715-chr3:164154502..164155534,19	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOL1-4	chr3:164088402-164088464	XLOC_002899
2	lnc-OTOL1-4	chr3:164078868-164078917	XLOC_002899

Variant related genes	Relation type
MIR720	TF binding region
MIR720	CpG island

Extended variants
information (count: 4834 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:4834 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530231774	chr3:163968862-163968863	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs186237875	chr3:163968914-163968915	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs191554320	chr3:163968946-163968947	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534174795	chr3:163968982-163968983	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184243881	chr3:163969011-163969012	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs1321549	chr3:163969081-163969082	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs1575151	chr3:163969095-163969096	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188599805	chr3:163969148-163969149	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs550493049	chr3:163969156-163969157	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547961111	chr3:163969159-163969160	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576103808	chr3:163969186-163969187	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545180996	chr3:163969287-163969288	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs571910499	chr3:163969358-163969359	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565035059	chr3:163969361-163969362	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570265067	chr3:163969397-163969398	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192742807	chr3:163969412-163969413	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541306031	chr3:163969461-163969462	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182107407	chr3:163969469-163969470	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561199631	chr3:163969506-163969507	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186571613	chr3:163969508-163969509	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549153307	chr3:163969536-163969537	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs191814442	chr3:163969639-163969640	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs183951416	chr3:163969703-163969704	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187525660	chr3:163969747-163969748	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35614057	chr3:163969749-163969750	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs73154464	chr3:163969765-163969766	Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs34665370	chr3:163969782-163969783	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs116030029	chr3:163969784-163969785	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544057593	chr3:163969829-163969830	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141843706	chr3:163969842-163969843	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs538900544	chr3:163969862-163969863	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs567647520	chr3:163969864-163969865	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs192807804	chr3:163969935-163969936	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs555927082	chr3:163969977-163969978	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs67669759	chr3:163970031-163970032	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs398052412	chr3:163970036-163970037	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115902188	chr3:163970101-163970102	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs150631741	chr3:163970145-163970146	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116372083	chr3:163970153-163970154	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572252029	chr3:163970163-163970164	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541253809	chr3:163970201-163970202	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554898239	chr3:163970204-163970205	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185727299	chr3:163970217-163970218	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190254434	chr3:163970230-163970231	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180993843	chr3:163970253-163970254	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs183897205	chr3:163970270-163970271	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs554498864	chr3:163970297-163970298	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138823606	chr3:163970310-163970311	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145252037	chr3:163970324-163970325	Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372950499	chr3:163970325-163970326	Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	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
Basal cell lymphoma	21115979	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16547154	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Sudden cardiac death	19188705	CNVD
Mantle cell lymphoma	19029149	CNVD
Malformation	19546859	CNVD
Schizophrenia	19546859	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Alcoholism	21790672	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	19651600	CNVD
Autism	19287141	CNVD
Incontinentia Pigmenti	22033527	CNVD
Rett syndrome	21593744	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Glioma	20126413	CNVD
Recurrent pregnancy loss	19789632	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163963200-163995200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:163979000-163996200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:163982400-163983200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr3:163990800-163993200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:163994400-163995200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr3:163995200-164000600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:163996200-163997000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
8	chr3:164000600-164002200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr3:164002200-164003000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr3:164003000-164005600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:164005600-164006800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:164006800-164007200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:164007200-164007600	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr3:164007600-164009400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:164009400-164009800	Active TSS	ES-I3 Cell Line	embryonic stem cell
16	chr3:164009400-164009800	Active TSS	H9 Cell Line	embryonic stem cell
17	chr3:164009400-164009800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr3:164009800-164014200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:164014200-164015400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr3:164015400-164017000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:164017000-164017400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:164017400-164019800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:164018200-164019000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr3:164019800-164020400	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:164020400-164023200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:164023200-164025000	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:164025000-164026000	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:164026000-164026600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:164026600-164031400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:164027000-164027200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
31	chr3:164027400-164028200	Weak transcription	Pancreatic Islets	Pancreatic Islet
32	chr3:164031400-164033800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:164033800-164034800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:164034800-164035400	Genic enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:164035400-164035600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr3:164035600-164036200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:164036200-164038400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:164038400-164038600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:164038400-164039400	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr3:164038400-164042400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:164038600-164038800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr3:164038600-164039200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr3:164038600-164039200	Enhancers	H9 Cell Line	embryonic stem cell
44	chr3:164038600-164039200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr3:164038600-164039400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr3:164038600-164039400	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr3:164038600-164039400	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr3:164038600-164039600	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr3:164038600-164039800	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr3:164038800-164039000	Enhancers	ES-I3 Cell Line	embryonic stem cell

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