Variant report

Variant	nsv1021065
Chromosome Location	chr8:3439221-3492246
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	BACH1	chr8:3491473-3491649	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL3	chr8:3456830-3457201	GM12878	blood:	n/a	n/a
3	CEBPB	chr8:3475245-3475445	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr8:3486970-3487053	HepG2	liver:	n/a	chr8:3487017-3487028 chr8:3487015-3487026
5	CEBPB	chr8:3458334-3458381	A549	lung:	n/a	n/a
6	CEBPB	chr8:3475205-3475329	HepG2	liver:	n/a	n/a
7	CEBPD	chr8:3449018-3449462	K562	blood:	n/a	n/a
8	CTCF	chr8:3442475-3442819	K562	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
9	CTCF	chr8:3442590-3442729	GM10248	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
10	CTCF	chr8:3442620-3442770	GM06990	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
11	CTCF	chr8:3478620-3478770	GM12869	blood:	n/a	n/a
12	CTCF	chr8:3442580-3442730	GM12873	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
13	CTCF	chr8:3442544-3442707	MCF-7	breast:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
14	CTCF	chr8:3442446-3442784	K562	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
15	CTCF	chr8:3442600-3442750	WERI-Rb-1	eye:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
16	CTCF	chr8:3442520-3442728	GM12891	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
17	CTCF	chr8:3442557-3442722	ProgFib	skin:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
18	CTCF	chr8:3442520-3442670	GM12873	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
19	CTCF	chr8:3442540-3442690	GM12875	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
20	CTCF	chr8:3442587-3442729	Hela-S3	cervix:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
21	CTCF	chr8:3442547-3442751	GM12878	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
22	CTCF	chr8:3442600-3442750	Hela-S3	cervix:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
23	CTCF	chr8:3442600-3442750	GM12866	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
24	CTCF	chr8:3442440-3442590	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr8:3442520-3442670	HCFaa	heart:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
26	CTCF	chr8:3442420-3442570	HCT-116	colon:	n/a	n/a
27	CTCF	chr8:3442653-3442689	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr8:3442510-3442776	A549	lung:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
29	CTCF	chr8:3442540-3442690	AG04449	skin:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
30	CTCF	chr8:3442466-3442753	H1-hESC	embryonic stem cell:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
31	CTCF	chr8:3442580-3442730	GM12868	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
32	CTCF	chr8:3442600-3442750	SK-N-SH_RA	brain:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
33	CTCF	chr8:3442560-3442710	HRPEpiC	eye:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
34	CTCF	chr8:3442452-3442764	K562	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
35	CTCF	chr8:3442540-3442690	HPAF	blood vessel:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
36	CTCF	chr8:3442660-3442810	GM12871	blood:	n/a	n/a
37	CTCF	chr8:3442453-3442729	K562	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
38	CTCF	chr8:3442480-3442735	SK-N-SH_RA	brain:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
39	CTCF	chr8:3442640-3442790	HAc	cerebellar:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657
40	CTCF	chr8:3442620-3442770	WERI-Rb-1	eye:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
41	CTCF	chr8:3486020-3486170	GM12866	blood:	n/a	n/a
42	CTCF	chr8:3442620-3442770	GM12869	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
43	CTCF	chr8:3442680-3442830	HFF	foreskin:	n/a	n/a
44	CTCF	chr8:3442580-3442730	HMEC	breast:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
45	CTCF	chr8:3442380-3442530	HFF	foreskin:	n/a	n/a
46	CTCF	chr8:3442036-3442096	GM13976	blood:	n/a	n/a
47	CTCF	chr8:3442263-3442950	SK-N-SH	brain:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
48	CTCF	chr8:3442520-3442670	HBMEC	blood vessel:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658
49	CTCF	chr8:3442660-3442810	HFF-Myc	foreskin:	n/a	n/a
50	CTCF	chr8:3442468-3442820	GM12878	blood:	n/a	chr8:3442643-3442659 chr8:3442642-3442660 chr8:3442648-3442657 chr8:3442637-3442658

No.	Distal block	Cell Line	Cell type
1	chr8:3482781..3484971-chr8:3489836..3491508,2	K562	blood:
2	chr8:3482781..3484971-chr8:3489836..3491508,2	K562	blood:
3	chr8:3142043..3142754-chr8:3442196..3443079,3	K562	blood:
4	chr12:58159481..58160161-chr8:3442277..3442945,2	HCT-116	colon:

Variant related genes	Relation type
CSMD1	TF binding region
ENSG00000183117	chromatin interactions

Extended variants
information (count: 2111 )
Associated
traits (count: 125 )

Variant overlapped rSNPs/rCNVs (count:2111 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148170225	chr8:3440617-3440618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs113814047	chr8:3440657-3440658	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs986946	chr8:3440664-3440665	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs986947	chr8:3440678-3440679	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs141073204	chr8:3440693-3440694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182955967	chr8:3440704-3440705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs186005587	chr8:3440719-3440720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539007018	chr8:3440733-3440734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567507519	chr8:3440763-3440764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs572103305	chr8:3440790-3440791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs4875739	chr8:3440833-3440834	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs986948	chr8:3440839-3440840	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs191145689	chr8:3440843-3440844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs150251035	chr8:3440846-3440847	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573491865	chr8:3440847-3440848	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4875740	chr8:3440851-3440852	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs565207368	chr8:3440856-3440857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139210515	chr8:3440879-3440880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs183456062	chr8:3440891-3440892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs142770640	chr8:3440892-3440893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530628629	chr8:3440894-3440895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548936986	chr8:3440895-3440896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs147372448	chr8:3440899-3440900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73660312	chr8:3440913-3440914	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs137954733	chr8:3440917-3440918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs563645659	chr8:3440931-3440932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs571520873	chr8:3440933-3440934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs539045665	chr8:3440939-3440940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs532555385	chr8:3440945-3440946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550948538	chr8:3440956-3440957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs569279631	chr8:3440959-3440960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs4875741	chr8:3440960-3440961	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73489503	chr8:3440972-3440973	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs187449075	chr8:3440975-3440976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192739964	chr8:3440978-3440979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs566367341	chr8:3440984-3440985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372068729	chr8:3441015-3441016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs577114438	chr8:3441031-3441032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs544653500	chr8:3441043-3441044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149454993	chr8:3441056-3441057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs114823676	chr8:3441072-3441073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs183712243	chr8:3441089-3441090	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs567938156	chr8:3441096-3441097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs578148298	chr8:3441099-3441100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs11994822	chr8:3441104-3441105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs375394860	chr8:3441145-3441146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs12680424	chr8:3441164-3441165	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs546778523	chr8:3441173-3441174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11994081	chr8:3441174-3441175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs12681886	chr8:3441189-3441190	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:125)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
abnormal development	18461090	CNVD
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Ductal carcinoma	22052326	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Epilepsy	22083797	CNVD
Acute myeloid leukemia	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Autism	22495311	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Ovarian cancer	22355333	CNVD
Breast cancer	21364760	CNVD
Cancer	20164920	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21829676	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Prostate cancer	17217626	CNVD
Developmental delay	19128483	CNVD
Neuroticism	17667963	CNVD
Leukoplakia	24403051	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Schizophrenia	19805367	CNVD
Colorectal cancer	16774939	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	22014273	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:3440600-3441200	Enhancers	Fetal Heart	heart
2	chr8:3440600-3441400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr8:3442400-3442800	Enhancers	Brain Cingulate Gyrus	brain
4	chr8:3443600-3445200	Enhancers	Fetal Muscle Leg	muscle
5	chr8:3450400-3450600	Enhancers	Fetal Muscle Trunk	muscle
6	chr8:3450600-3453400	Weak transcription	Fetal Muscle Trunk	muscle
7	chr8:3451600-3451800	Enhancers	Fetal Lung	lung
8	chr8:3452000-3452400	Enhancers	Brain Cingulate Gyrus	brain
9	chr8:3452000-3452600	Enhancers	Brain Hippocampus Middle	brain
10	chr8:3452200-3452400	Enhancers	Gastric	stomach
11	chr8:3452200-3453400	Enhancers	Brain Anterior Caudate	brain
12	chr8:3452200-3453800	Enhancers	Brain Angular Gyrus	brain
13	chr8:3452200-3454800	Enhancers	Fetal Muscle Leg	muscle
14	chr8:3452400-3452600	Flanking Active TSS	Brain Cingulate Gyrus	brain
15	chr8:3452400-3454800	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr8:3452600-3453000	Active TSS	Brain Hippocampus Middle	brain
17	chr8:3452600-3453000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
18	chr8:3452600-3453400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr8:3452600-3453800	Enhancers	Brain Cingulate Gyrus	brain
20	chr8:3452800-3453600	Enhancers	Brain Substantia Nigra	brain
21	chr8:3453000-3453600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr8:3453000-3453800	Enhancers	Brain Hippocampus Middle	brain
23	chr8:3453200-3453800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr8:3453400-3454400	Enhancers	Fetal Lung	lung
25	chr8:3453400-3454800	Enhancers	Fetal Muscle Trunk	muscle
26	chr8:3454200-3454600	Enhancers	Gastric	stomach
27	chr8:3462800-3464600	Weak transcription	Fetal Heart	heart
28	chr8:3464600-3465400	Enhancers	Fetal Heart	heart
29	chr8:3471800-3479800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr8:3479800-3480000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr8:3485400-3487800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:3487600-3488600	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr8:3487800-3488000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr8:3488000-3488200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr8:3488200-3488600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr8:3488600-3489400	Enhancers	Fetal Heart	heart
37	chr8:3490400-3491200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr8:3491600-3492200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:3492000-3493000	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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