Variant report

Variant	esv2757902
Chromosome Location	chr3:162471049-162742794
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:676)
CpG islands
(count:245)
Chromatin interactive
region (count:28)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:162547298-162547407	K562	blood:	n/a	n/a
2	BACH1	chr3:162650431-162650615	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr3:162610898-162611612	A549	lung:	n/a	chr3:162611348-162611357
4	BRCA1	chr3:162717002-162717061	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr3:162490538-162490834	HepG2	liver:	n/a	chr3:162490691-162490702
6	CEBPB	chr3:162711839-162712097	IMR90	lung:	n/a	chr3:162711927-162711938
7	CEBPB	chr3:162628264-162628508	A549	lung:	n/a	chr3:162628401-162628412
8	CEBPB	chr3:162493987-162494268	A549	lung:	n/a	n/a
9	CEBPB	chr3:162493941-162494308	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr3:162537323-162537439	HepG2	liver:	n/a	chr3:162537366-162537383 chr3:162537369-162537380 chr3:162537369-162537382 chr3:162537369-162537382 chr3:162537371-162537382 chr3:162537369-162537382
11	CEBPB	chr3:162628262-162628535	IMR90	lung:	n/a	chr3:162628401-162628412
12	CEBPB	chr3:162695972-162696288	IMR90	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
13	CEBPB	chr3:162581342-162581834	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:162729220-162729874	MCF-7	breast:	n/a	n/a
15	CEBPB	chr3:162695964-162696261	HepG2	liver:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
16	CEBPB	chr3:162682143-162682476	HepG2	liver:	n/a	chr3:162682288-162682299
17	CEBPB	chr3:162544112-162544312	HepG2	liver:	n/a	chr3:162544161-162544172
18	CEBPB	chr3:162729522-162729600	A549	lung:	n/a	n/a
19	CEBPB	chr3:162729383-162729666	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr3:162695893-162696380	MCF-7	breast:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
21	CEBPB	chr3:162695952-162696294	A549	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
22	CEBPB	chr3:162682141-162682443	A549	lung:	n/a	chr3:162682288-162682299
23	CEBPB	chr3:162696009-162696307	A549	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
24	CEBPB	chr3:162611223-162611631	A549	lung:	n/a	n/a
25	CEBPB	chr3:162696021-162696193	K562	blood:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
26	CEBPB	chr3:162611102-162611541	A549	lung:	n/a	n/a
27	CEBPB	chr3:162493943-162494295	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr3:162729049-162729851	MCF-7	breast:	n/a	n/a
29	CEBPB	chr3:162628256-162628557	HepG2	liver:	n/a	chr3:162628401-162628412
30	CEBPB	chr3:162491565-162491768	A549	lung:	n/a	n/a
31	CEBPB	chr3:162682187-162682344	K562	blood:	n/a	chr3:162682288-162682299
32	CEBPB	chr3:162610699-162611670	A549	lung:	n/a	n/a
33	CEBPB	chr3:162695846-162696372	A549	lung:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
34	CEBPB	chr3:162695938-162696308	MCF-7	breast:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
35	CEBPB	chr3:162493953-162494306	IMR90	lung:	n/a	n/a
36	CEBPB	chr3:162476750-162477034	IMR90	lung:	n/a	chr3:162476875-162476886
37	CEBPB	chr3:162476766-162477058	A549	lung:	n/a	chr3:162476875-162476886
38	CEBPB	chr3:162571076-162571241	A549	lung:	n/a	n/a
39	CEBPB	chr3:162729092-162729733	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr3:162682128-162682457	IMR90	lung:	n/a	chr3:162682288-162682299
41	CEBPB	chr3:162695982-162696258	H1-hESC	embryonic stem cell:	n/a	chr3:162696130-162696139 chr3:162696130-162696139 chr3:162696130-162696139
42	CEBPB	chr3:162476765-162477042	HepG2	liver:	n/a	chr3:162476875-162476886
43	CEBPB	chr3:162581432-162581699	MCF-7	breast:	n/a	n/a
44	CEBPB	chr3:162711790-162712125	HepG2	liver:	n/a	chr3:162711927-162711938
45	CHD2	chr3:162492211-162492255	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr3:162565400-162565550	AG09319	gingival:	n/a	n/a
47	CTCF	chr3:162478360-162478510	Caco-2	colon:	n/a	n/a
48	CTCF	chr3:162495020-162495170	AG04450	lung:	n/a	n/a
49	CTCF	chr3:162517800-162517950	AG04449	skin:	n/a	n/a
50	CTCF	chr3:162583360-162583510	MCF-7	breast:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:162705427-162705477	PrEC	prostate:	n/a
2	chr3:162705427-162705477	PrEC	prostate:	n/a
3	chr3:162653787-162653837	Caco-2	colon:	n/a
4	chr3:162705203-162705253	H1-hESC	embryonic stem cell:	embryo
5	chr3:162653787-162653837	HAEpiC	amniotic membrane:	n/a
6	chr3:162653787-162653837	BE2_C	brain:	n/a
7	chr3:162653787-162653837	HRCEpiC	kidney:	n/a
8	chr3:162705427-162705477	Hepatocyte	liver:	n/a
9	chr3:162705337-162705387	SKMC	muscle:	n/a
10	chr3:162705337-162705387	BE2_C	brain:	n/a
11	chr3:162705203-162705253	BJ	skin:	n/a
12	chr3:162705427-162705477	HEK293	kidney:	embryo
13	chr3:162653787-162653837	HCPEpiC	choroid plexus:	n/a
14	chr3:162705427-162705477	HCM	heart:	n/a
15	chr3:162653787-162653837	SK-N-MC	brain:	n/a
16	chr3:162705427-162705477	IMR90	lung:	fetal
17	chr3:162653787-162653837	PrEC	prostate:	n/a
18	chr3:162653787-162653837	GM06990	blood:	n/a
19	chr3:162653787-162653837	H1-hESC	embryonic stem cell:	embryo
20	chr3:162705337-162705387	HEEpiC	esophagus:	n/a
21	chr3:162705203-162705253	Hepatocyte	liver:	n/a
22	chr3:162705203-162705253	ovcar-3	ovarian:	n/a
23	chr3:162705203-162705253	SK-N-SH	brain:	n/a
24	chr3:162653787-162653837	T-47D	breast:	n/a
25	chr3:162705337-162705387	U87	brain:	n/a
26	chr3:162653787-162653837	AG09309	skin:	n/a
27	chr3:162705203-162705253	GM19239	blood:	n/a
28	chr3:162705427-162705477	T-47D	breast:	n/a
29	chr3:162705203-162705253	PFSK-1	brain:	n/a
30	chr3:162705203-162705253	Caco-2	colon:	n/a
31	chr3:162653787-162653837	Jurkat	blood:	n/a
32	chr3:162653787-162653837	HepG2	liver:	n/a
33	chr3:162705337-162705387	HPAEpiC	pulmonary alveolar:	n/a
34	chr3:162705337-162705387	SK-N-SH	brain:	n/a
35	chr3:162705337-162705387	NHDF-neo	bronchial:	n/a
36	chr3:162705427-162705477	AoSMC	blood vessel:	n/a
37	chr3:162705427-162705477	HL-60	blood:	n/a
38	chr3:162653787-162653837	ProgFib	skin:	n/a
39	chr3:162705203-162705253	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:162705427-162705477	ECC-1	luminal epithelium:	n/a
41	chr3:162705337-162705387	K562	blood:	n/a
42	chr3:162705337-162705387	Hepatocyte	liver:	n/a
43	chr3:162705203-162705253	AG04449	skin:	fetal
44	chr3:162705203-162705253	AG09309	skin:	n/a
45	chr3:162705203-162705253	Jurkat	blood:	n/a
46	chr3:162653787-162653837	HUVEC	blood vessel:	n/a
47	chr3:162705427-162705477	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:162705203-162705253	K562	blood:	n/a
49	chr3:162705427-162705477	BJ	skin:	n/a
50	chr3:162705427-162705477	ovcar-3	ovarian:	n/a

(count:28 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:162554556..162557102-chr3:162558855..162561328,2	K562	blood:
2	chr3:162524861..162526931-chr3:162547103..162549053,2	MCF-7	breast:
3	chr3:162627188..162629037-chr3:162630724..162633448,2	MCF-7	breast:
4	chr20:11421691..11422663-chr3:162694553..162695419,2	MCF-7	breast:
5	chr3:162554556..162557102-chr3:162558855..162561328,2	K562	blood:
6	chr3:162627188..162629037-chr3:162630724..162633448,2	MCF-7	breast:
7	chr3:162548004..162549875-chr3:162551679..162554489,2	MCF-7	breast:
8	chr3:162118223..162119105-chr3:162517137..162517997,2	MCF-7	breast:
9	chr3:162622047..162623612-chr3:162639605..162642211,2	K562	blood:
10	chr3:162524861..162526931-chr3:162547103..162549053,2	MCF-7	breast:
11	chr3:162548004..162549875-chr3:162551679..162554489,2	MCF-7	breast:
12	chr3:162468849..162471720-chr3:162897232..162899564,2	K562	blood:
13	chr14:60627662..60628534-chr3:162740219..162740719,2	MCF-7	breast:
14	chr3:162494680..162495563-chr3:162760633..162761552,3	MCF-7	breast:
15	chr3:162692633..162695202-chr3:162700914..162703834,2	MCF-7	breast:
16	chr3:162475543..162478495-chr3:162480272..162482533,2	MCF-7	breast:
17	chr3:162695238..162696118-chr5:168564460..168564967,2	MCF-7	breast:
18	chr3:162622047..162623612-chr3:162639605..162642211,2	K562	blood:
19	chr3:162471864..162474454-chr3:162482441..162485010,2	MCF-7	breast:
20	chr3:162475543..162478495-chr3:162480272..162482533,2	MCF-7	breast:
21	chr3:162471864..162474454-chr3:162482441..162485010,2	MCF-7	breast:
22	chr3:162486396..162487274-chr3:162497260..162497768,2	MCF-7	breast:
23	chr16:87583669..87584291-chr3:162551047..162551567,2	MCF-7	breast:
24	chr3:162692633..162695202-chr3:162700914..162703834,2	MCF-7	breast:
25	chr16:87583726..87584390-chr3:162551047..162551567,2	MCF-7	breast:
26	chr3:162486396..162487274-chr3:162497260..162497768,2	MCF-7	breast:
27	chr3:162730866..162732605-chr3:162732763..162734314,2	MCF-7	breast:
28	chr3:162730866..162732605-chr3:162732763..162734314,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OTOL1-2	chr3:162631870-162632022	NONHSAT093026

No data

Variant related genes	Relation type
ENSG00000241168	TF binding region
ENSG00000241168	CpG island

Extended variants
information (count: 5265 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:5265 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs140896372	chr3:162471059-162471060	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566645359	chr3:162471062-162471063	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150175052	chr3:162471096-162471097	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs113339857	chr3:162471103-162471104	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555371811	chr3:162471110-162471111	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs193021669	chr3:162471173-162471174	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs537973890	chr3:162471191-162471192	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs138137633	chr3:162471199-162471200	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs67171011	chr3:162471233-162471234	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs202229970	chr3:162471235-162471236	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs200223200	chr3:162471236-162471237	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372985241	chr3:162471237-162471238	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs578156109	chr3:162471270-162471271	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs6441551	chr3:162471292-162471293	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs554454472	chr3:162471299-162471300	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78135478	chr3:162471334-162471335	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542635574	chr3:162471380-162471381	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs377724998	chr3:162471386-162471387	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs149573202	chr3:162471414-162471415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183332593	chr3:162471426-162471427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545515809	chr3:162471560-162471561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs555477557	chr3:162471565-162471566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs371139959	chr3:162471575-162471576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs13073470	chr3:162471626-162471627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs200633116	chr3:162471642-162471643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368428497	chr3:162471644-162471645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59237780	chr3:162471645-162471646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs67925967	chr3:162471646-162471647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199860136	chr3:162471647-162471648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199575541	chr3:162471648-162471649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200772268	chr3:162471650-162471651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201760998	chr3:162471652-162471653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs1845910	chr3:162471683-162471684	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs533195567	chr3:162471685-162471686	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs546438312	chr3:162471703-162471704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73016487	chr3:162471717-162471718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs71625443	chr3:162471726-162471727	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs146551713	chr3:162471750-162471751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs186571144	chr3:162471847-162471848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35740589	chr3:162471899-162471900	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs112931604	chr3:162471915-162471916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs35822825	chr3:162471965-162471966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs79009008	chr3:162471977-162471978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532236319	chr3:162471978-162471979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs397991516	chr3:162471979-162471980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530561065	chr3:162472059-162472060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527325245	chr3:162472084-162472085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557874545	chr3:162472087-162472088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191403744	chr3:162472098-162472099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143168390	chr3:162472102-162472103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
Breast cancer	21364760	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
Chordoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:162470200-162471400	Strong transcription	ES-I3 Cell Line	embryonic stem cell
2	chr3:162470800-162480400	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr3:162471400-162480400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr3:162473200-162473600	Enhancers	Dnd41	blood
5	chr3:162473600-162475200	Weak transcription	Dnd41	blood
6	chr3:162475200-162475600	Enhancers	Dnd41	blood
7	chr3:162480200-162481000	Enhancers	Dnd41	blood
8	chr3:162480400-162481200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr3:162480400-162482000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:162481000-162483200	Weak transcription	Dnd41	blood
11	chr3:162481200-162482400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr3:162481200-162483400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr3:162481400-162481600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr3:162481600-162492200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
15	chr3:162481800-162482400	Enhancers	Fetal Intestine Large	intestine
16	chr3:162482200-162482800	Enhancers	NHDF-Ad	bronchial
17	chr3:162482400-162482800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr3:162482400-162483400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:162482800-162487000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:162483200-162484400	ZNF genes & repeats	Dnd41	blood
21	chr3:162483400-162484000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr3:162483400-162484200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:162483400-162484400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
24	chr3:162483400-162485200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:162483600-162484200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr3:162484200-162484600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr3:162484400-162490200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr3:162485000-162485200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr3:162485200-162487000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr3:162485200-162492200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr3:162487000-162487600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr3:162487000-162489200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr3:162487600-162489000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr3:162489000-162490000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr3:162490000-162492400	Genic enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr3:162490200-162491400	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr3:162491200-162493400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:162491400-162493200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
39	chr3:162491400-162493400	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr3:162491400-162493800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:162491600-162493200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr3:162492000-162493200	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr3:162492000-162493400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr3:162492000-162494400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr3:162492200-162492800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
46	chr3:162492200-162492800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:162492400-162493000	Enhancers	Dnd41	blood
48	chr3:162492400-162493200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr3:162492800-162493400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:162493000-162494600	Weak transcription	Dnd41	blood

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