Variant report

Variant	nsv1006270
Chromosome Location	chr3:163651905-163849686
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	BRCA1	chr3:163722192-163722316	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr3:163766344-163766626	MCF-7	breast:	n/a	chr3:163766435-163766446
3	CEBPB	chr3:163811615-163811972	Hela-S3	cervix:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
4	CEBPB	chr3:163766249-163766626	A549	lung:	n/a	chr3:163766435-163766446
5	CEBPB	chr3:163767676-163768024	Hela-S3	cervix:	n/a	chr3:163767891-163767904
6	CEBPB	chr3:163766257-163766618	HepG2	liver:	n/a	chr3:163766435-163766446
7	CEBPB	chr3:163657645-163657992	MCF-7	breast:	n/a	n/a
8	CEBPB	chr3:163766296-163766594	H1-hESC	embryonic stem cell:	n/a	chr3:163766435-163766446
9	CEBPB	chr3:163811718-163811889	H1-hESC	embryonic stem cell:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
10	CEBPB	chr3:163811663-163811965	MCF-7	breast:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
11	CEBPB	chr3:163767753-163767980	HepG2	liver:	n/a	chr3:163767891-163767904
12	CEBPB	chr3:163776828-163777158	HepG2	liver:	n/a	chr3:163777001-163777012
13	CEBPB	chr3:163766262-163766585	K562	blood:	n/a	chr3:163766435-163766446
14	CEBPB	chr3:163766342-163766605	ECC-1	luminal epithelium:	n/a	chr3:163766435-163766446
15	CEBPB	chr3:163805104-163805270	HepG2	liver:	n/a	chr3:163805134-163805145
16	CEBPB	chr3:163776930-163777140	H1-hESC	embryonic stem cell:	n/a	chr3:163777001-163777012
17	CEBPB	chr3:163722123-163722274	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr3:163776822-163777172	IMR90	lung:	n/a	chr3:163777001-163777012
19	CEBPB	chr3:163765379-163765657	HepG2	liver:	n/a	chr3:163765471-163765482
20	CEBPB	chr3:163811617-163811939	HepG2	liver:	n/a	chr3:163811787-163811796 chr3:163811785-163811796
21	CEBPB	chr3:163742739-163742774	A549	lung:	n/a	n/a
22	CEBPB	chr3:163800790-163801049	HepG2	liver:	n/a	chr3:163800890-163800901
23	CEBPB	chr3:163766254-163766629	IMR90	lung:	n/a	chr3:163766435-163766446
24	CEBPB	chr3:163766280-163766585	Hela-S3	cervix:	n/a	chr3:163766435-163766446
25	CEBPB	chr3:163776817-163777197	A549	lung:	n/a	chr3:163777001-163777012
26	CEBPB	chr3:163765442-163765609	A549	lung:	n/a	chr3:163765471-163765482
27	CHD2	chr3:163722101-163722388	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr3:163669284-163669460	HepG2	liver:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
29	CTCF	chr3:163722240-163722390	NB4	blood:	n/a	chr3:163722244-163722257
30	CTCF	chr3:163657980-163658130	Hela-S3	cervix:	n/a	n/a
31	CTCF	chr3:163722086-163722401	H1-hESC	embryonic stem cell:	n/a	chr3:163722244-163722257
32	CTCF	chr3:163670533-163670540	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:163657940-163658090	Hela-S3	cervix:	n/a	n/a
34	CTCF	chr3:163657912-163658101	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:163657840-163657990	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr3:163657940-163658090	HA-sp	spinal cord:	n/a	n/a
37	CTCF	chr3:163674887-163675245	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:163669300-163669450	RPTEC	kidney:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
39	CTCF	chr3:163669180-163669330	HAc	cerebellar:	n/a	n/a
40	CTCF	chr3:163658000-163658150	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr3:163669295-163669493	Pancreas_OC	pancreas:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
42	CTCF	chr3:163669260-163669410	NHEK	skin:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
43	CTCF	chr3:163669280-163669430	RPTEC	kidney:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
44	CTCF	chr3:163658000-163658150	SAEC	small airway:	n/a	n/a
45	CTCF	chr3:163669314-163669473	MCF-7	breast:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
46	CTCF	chr3:163669260-163669410	HPAF	blood vessel:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
47	CTCF	chr3:163729568-163729594	MCF-7	breast:	n/a	n/a
48	CTCF	chr3:163669300-163669450	HL-60	blood:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392
49	CTCF	chr3:163657920-163658070	HBMEC	blood vessel:	n/a	n/a
50	CTCF	chr3:163669065-163669645	HCT-116	colon:	n/a	chr3:163669376-163669394 chr3:163669377-163669393 chr3:163669371-163669392

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:163722051-163722101	SK-N-SH_RA	brain:	n/a
2	chr3:163719428-163719478	HCM	heart:	n/a
3	chr3:163719236-163719286	HNPCEpiC	eye:	n/a
4	chr3:163719428-163719478	HAEpiC	amniotic membrane:	n/a
5	chr3:163722208-163722258	GM06990	blood:	n/a
6	chr3:163722051-163722101	Hela-S3	cervix:	n/a
7	chr3:163719236-163719286	SK-N-SH	brain:	n/a
8	chr3:163722051-163722101	HRCEpiC	kidney:	n/a
9	chr3:163719236-163719286	HCM	heart:	n/a
10	chr3:163722208-163722258	SK-N-SH_RA	brain:	n/a
11	chr3:163722051-163722101	ECC-1	luminal epithelium:	n/a
12	chr3:163722208-163722258	HRCEpiC	kidney:	n/a
13	chr3:163719236-163719286	AG09309	skin:	n/a
14	chr3:163722051-163722101	HRPEpiC	eye:	n/a
15	chr3:163719428-163719478	MCF-7	breast:	n/a
16	chr3:163719236-163719286	HEK293	kidney:	embryo
17	chr3:163722208-163722258	HNPCEpiC	eye:	n/a
18	chr3:163722294-163722344	CMK	blood:	n/a
19	chr3:163722208-163722258	K562	blood:	n/a
20	chr3:163722294-163722344	HAEpiC	amniotic membrane:	n/a
21	chr3:163719428-163719478	PrEC	prostate:	n/a
22	chr3:163719428-163719478	HCF	heart:	n/a
23	chr3:163722294-163722344	HNPCEpiC	eye:	n/a
24	chr3:163722051-163722101	HUVEC	blood vessel:	n/a
25	chr3:163722294-163722344	AG09319	gingival:	n/a
26	chr3:163722208-163722258	LNCaP	prostate:	n/a
27	chr3:163719428-163719478	GM06990	blood:	n/a
28	chr3:163722208-163722258	HEEpiC	esophagus:	n/a
29	chr3:163722051-163722101	RPTEC	kidney:	n/a
30	chr3:163722294-163722344	SK-N-SH_RA	brain:	n/a
31	chr3:163722294-163722344	LNCaP	prostate:	n/a
32	chr3:163719236-163719286	HCPEpiC	choroid plexus:	n/a
33	chr3:163719236-163719286	NB4	blood:	n/a
34	chr3:163722294-163722344	GM19239	blood:	n/a
35	chr3:163722208-163722258	HAEpiC	amniotic membrane:	n/a
36	chr3:163722208-163722258	NHBE	bronchial:	n/a
37	chr3:163722294-163722344	NB4	blood:	n/a
38	chr3:163719428-163719478	HRCEpiC	kidney:	n/a
39	chr3:163722208-163722258	Caco-2	colon:	n/a
40	chr3:163722294-163722344	HPAEpiC	pulmonary alveolar:	n/a
41	chr3:163722294-163722344	SK-N-MC	brain:	n/a
42	chr3:163719236-163719286	AG04449	skin:	fetal
43	chr3:163719236-163719286	HRPEpiC	eye:	n/a
44	chr3:163722294-163722344	HRCEpiC	kidney:	n/a
45	chr3:163722294-163722344	ProgFib	skin:	n/a
46	chr3:163722051-163722101	GM12892	blood:	n/a
47	chr3:163719236-163719286	MCF-7	breast:	n/a
48	chr3:163719428-163719478	AG09309	skin:	n/a
49	chr3:163722208-163722258	AG09309	skin:	n/a
50	chr3:163722051-163722101	HepG2	liver:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:163759624..163761925-chr3:163765313..163767072,2	MCF-7	breast:
2	chr3:163660440..163662829-chr3:163666000..163668542,2	K562	blood:
3	chr3:163639924..163641654-chr3:163663861..163665823,2	MCF-7	breast:
4	chr3:163738641..163741233-chr3:163742705..163744722,2	MCF-7	breast:
5	chr1:219388883..219389633-chr3:163652052..163652630,2	MCF-7	breast:
6	chr15:52587462..52588981-chr3:163831086..163833177,2	MCF-7	breast:
7	chr3:163676571..163679360-chr3:163699055..163700602,2	MCF-7	breast:
8	chr3:163660440..163662829-chr3:163666000..163668542,2	K562	blood:
9	chr3:163816031..163818067-chr3:163819325..163821288,2	MCF-7	breast:
10	chr3:163741470..163744256-chr3:163747090..163749437,2	K562	blood:
11	chr3:163664276..163666199-chr3:163667456..163669439,2	MCF-7	breast:
12	chr3:163674728..163675758-chr3:164903457..164904093,3	MCF-7	breast:
13	chr3:163497409..163497997-chr3:163668939..163669921,2	MCF-7	breast:
14	chr3:163756511..163759205-chr3:163797731..163799263,2	MCF-7	breast:
15	chr3:163741470..163744256-chr3:163747090..163749437,2	K562	blood:
16	chr3:163831824..163833454-chr3:163836559..163838959,2	K562	blood:
17	chr3:163219408..163221189-chr3:163663438..163665910,2	K562	blood:
18	chr3:163816031..163818067-chr3:163819325..163821288,2	MCF-7	breast:
19	chr3:163647521..163649115-chr3:163652164..163654381,2	MCF-7	breast:
20	chr3:163674674..163675466-chr3:164524045..164524647,3	MCF-7	breast:
21	chr3:163634067..163635345-chr3:163668973..163669822,4	MCF-7	breast:
22	chr3:163689823..163692046-chr3:163703767..163706359,2	K562	blood:
23	chr3:163664276..163666199-chr3:163667456..163669439,2	MCF-7	breast:
24	chr3:163831824..163833454-chr3:163836559..163838959,2	K562	blood:
25	chr3:163756511..163759205-chr3:163797731..163799263,2	MCF-7	breast:
26	chr3:163759624..163761925-chr3:163765313..163767072,2	MCF-7	breast:
27	chr3:163689823..163692046-chr3:163703767..163706359,2	K562	blood:
28	chr3:163669046..163669790-chr3:164903266..164903861,2	MCF-7	breast:
29	chr14:86195432..86196215-chr3:163793960..163794780,2	MCF-7	breast:
30	chr3:163676571..163679360-chr3:163699055..163700602,2	MCF-7	breast:
31	chr3:163738641..163741233-chr3:163742705..163744722,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SI-6	chr3:163719394-163720253	NONHSAT093045

Variant related genes	Relation type
ENSG00000214210	TF binding region
ENSG00000214210	CpG island
ENSG00000128833	chromatin interactions

Extended variants
information (count: 5133 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:5133 , 50 per page) page: 1 2 3 4 5 6 7 ... 103

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7645490	chr3:163657804-163657805	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs577634069	chr3:163657848-163657849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs10936378	chr3:163657889-163657890	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs553017702	chr3:163657912-163657913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570794659	chr3:163657922-163657923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs572806782	chr3:163657932-163657933	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs3849461	chr3:163657933-163657934	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs555100693	chr3:163657969-163657970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561670246	chr3:163657986-163657987	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34761378	chr3:163658028-163658029	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544027010	chr3:163658074-163658075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564008556	chr3:163658136-163658137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs182460921	chr3:163658183-163658184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574219170	chr3:163670448-163670449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184283632	chr3:163670510-163670511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs80013016	chr3:163670527-163670528	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141609789	chr3:163670811-163670812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534881267	chr3:163670813-163670814	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs7627722	chr3:163670869-163670870	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs578197422	chr3:163670887-163670888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs574461898	chr3:163670891-163670892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs543470488	chr3:163670935-163670936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs369518729	chr3:163670953-163670954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs145365200	chr3:163670965-163670966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532505181	chr3:163670998-163670999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374782242	chr3:163671015-163671016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs552687568	chr3:163671032-163671033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs559977494	chr3:163671037-163671038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs9829001	chr3:163671071-163671072	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs548878755	chr3:163671074-163671075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7627791	chr3:163671095-163671096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537009461	chr3:163671105-163671106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs62284178	chr3:163671106-163671107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs570472921	chr3:163671108-163671109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539148792	chr3:163671145-163671146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201827503	chr3:163671148-163671149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572677101	chr3:163671164-163671165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs535285943	chr3:163671169-163671170	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs7630165	chr3:163671174-163671175	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs374134496	chr3:163671178-163671179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563531438	chr3:163671202-163671203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577209341	chr3:163671203-163671204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs7630237	chr3:163671228-163671229	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs561210153	chr3:163671239-163671240	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11710022	chr3:163671259-163671260	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs528669346	chr3:163671290-163671291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs551253872	chr3:163671319-163671320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs188896567	chr3:163671322-163671323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs112401967	chr3:163671330-163671331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs9829413	chr3:163671341-163671342	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:67)

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
Glioblastoma multiforme	21138945	CNVD
Cancer	20164919	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:163657800-163658200	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr3:163657800-163658200	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr3:163670400-163670600	Enhancers	Pancreas	Pancrea
4	chr3:163670800-163671200	Weak transcription	Pancreas	Pancrea
5	chr3:163671200-163671800	Enhancers	Pancreas	Pancrea
6	chr3:163671600-163671800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr3:163671800-163684800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:163686000-163686400	Active TSS	Gastric	stomach
9	chr3:163686200-163686600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr3:163719200-163719800	Enhancers	Fetal Stomach	stomach
11	chr3:163720600-163721200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr3:163721200-163721800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:163721800-163722000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:163722000-163722200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr3:163722200-163724600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr3:163724800-163727000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:163738600-163739200	Enhancers	Dnd41	blood
18	chr3:163739000-163739400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:163739400-163740400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr3:163740400-163740600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:163744200-163745800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr3:163745800-163749000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:163749000-163752600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr3:163752600-163754000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr3:163754000-163754400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr3:163754400-163757600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:163757600-163758400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr3:163758400-163771800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr3:163758600-163759400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:163758600-163759400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:163758600-163759800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr3:163759800-163761200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr3:163761400-163761600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:163763800-163764000	Enhancers	Placenta	Placenta
35	chr3:163764000-163768000	Weak transcription	Placenta	Placenta
36	chr3:163765800-163766000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:163766000-163766200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr3:163768000-163768200	Enhancers	Placenta	Placenta
39	chr3:163771800-163795600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:163795600-163796000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:163796000-163797400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr3:163797400-163798800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:163798800-163803400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:163803400-163804400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr3:163804400-163805400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr3:163805400-163806800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:163806800-163811400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:163811400-163814400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:163811800-163814400	Enhancers	Dnd41	blood
50	chr3:163814400-163832200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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