Variant report

Variant	esv3450283
Chromosome Location	chr8:39180844-39238225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:346)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:39184983-39185219	HepG2	liver:	n/a	n/a
2	ATF1	chr8:39187249-39187365	K562	blood:	n/a	n/a
3	ATF1	chr8:39204094-39204343	K562	blood:	n/a	n/a
4	ATF1	chr8:39184952-39185134	K562	blood:	n/a	n/a
5	BCL11A	chr8:39215146-39215389	GM12878	blood:	n/a	n/a
6	BCL11A	chr8:39215071-39215373	GM12878	blood:	n/a	n/a
7	CBX3	chr8:39184878-39185271	HCT-116	colon:	n/a	n/a
8	CEBPB	chr8:39225484-39225625	IMR90	lung:	n/a	n/a
9	CTCF	chr8:39184935-39185180	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr8:39185060-39185210	HL-60	blood:	n/a	n/a
11	CTCF	chr8:39184915-39185305	IMR90	lung:	n/a	n/a
12	CTCF	chr8:39185309-39185312	Spleen_OC	spleen:	n/a	n/a
13	CTCF	chr8:39185020-39185170	HUVEC	blood vessel:	n/a	n/a
14	CTCF	chr8:39184678-39185583	A549	lung:	n/a	n/a
15	CTCF	chr8:39185500-39185650	AG09309	skin:	n/a	n/a
16	CTCF	chr8:39225560-39225710	HCT-116	colon:	n/a	n/a
17	CTCF	chr8:39185343-39185423	Gliobla	brain:	n/a	n/a
18	CTCF	chr8:39185040-39185190	HPF	lung:	n/a	n/a
19	CTCF	chr8:39185000-39185150	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr8:39184847-39185284	K562	blood:	n/a	n/a
21	CTCF	chr8:39185020-39185170	SAEC	small airway:	n/a	n/a
22	CTCF	chr8:39185020-39185170	GM12867	blood:	n/a	n/a
23	CTCF	chr8:39225660-39225810	HCFaa	heart:	n/a	chr8:39225708-39225715 chr8:39225701-39225719 chr8:39225696-39225717
24	CTCF	chr8:39185040-39185190	GM12864	blood:	n/a	n/a
25	CTCF	chr8:39185360-39185510	GM06990	blood:	n/a	n/a
26	CTCF	chr8:39185040-39185190	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr8:39185029-39185195	Pancreas_OC	pancreas:	n/a	n/a
28	CTCF	chr8:39185000-39185150	GM12873	blood:	n/a	n/a
29	CTCF	chr8:39185338-39185436	K562	blood:	n/a	n/a
30	CTCF	chr8:39184920-39185070	HFF-Myc	foreskin:	n/a	n/a
31	CTCF	chr8:39184893-39185207	A549	lung:	n/a	n/a
32	CTCF	chr8:39184960-39185110	GM12873	blood:	n/a	n/a
33	CTCF	chr8:39185040-39185190	GM12872	blood:	n/a	n/a
34	CTCF	chr8:39184966-39185166	A549	lung:	n/a	n/a
35	CTCF	chr8:39184960-39185110	NHEK	skin:	n/a	n/a
36	CTCF	chr8:39185020-39185170	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr8:39185347-39185452	GM13977	blood:	n/a	n/a
38	CTCF	chr8:39185040-39185190	GM12878	blood:	n/a	n/a
39	CTCF	chr8:39185020-39185170	GM12870	blood:	n/a	n/a
40	CTCF	chr8:39185020-39185170	HCT-116	colon:	n/a	n/a
41	CTCF	chr8:39185020-39185170	RPTEC	kidney:	n/a	n/a
42	CTCF	chr8:39185021-39185186	GM13976	blood:	n/a	n/a
43	CTCF	chr8:39185380-39185530	GM12864	blood:	n/a	n/a
44	CTCF	chr8:39185040-39185190	GM12870	blood:	n/a	n/a
45	CTCF	chr8:39184932-39185242	GM12878	blood:	n/a	n/a
46	CTCF	chr8:39184960-39185110	GM12866	blood:	n/a	n/a
47	CTCF	chr8:39185348-39185444	GM12878	blood:	n/a	n/a
48	CTCF	chr8:39185006-39185159	Fibrobl	skin:	n/a	n/a
49	CTCF	chr8:39184803-39185311	HCT-116	colon:	n/a	n/a
50	CTCF	chr8:39185711-39185715	GM10266	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:39223182-39223232	AoSMC	blood vessel:	n/a
2	chr8:39196907-39196957	GM06990	blood:	n/a
3	chr8:39196907-39196957	Caco-2	colon:	n/a
4	chr8:39223182-39223232	RPTEC	kidney:	n/a
5	chr8:39223182-39223232	MCF-7	breast:	n/a
6	chr8:39223182-39223232	NB4	blood:	n/a
7	chr8:39196907-39196957	SAEC	small airway:	n/a
8	chr8:39196907-39196957	ProgFib	skin:	n/a
9	chr8:39223182-39223232	SKMC	muscle:	n/a
10	chr8:39223182-39223232	ECC-1	luminal epithelium:	n/a
11	chr8:39223182-39223232	PANC-1	pancreas:	n/a
12	chr8:39196907-39196957	HRPEpiC	eye:	n/a
13	chr8:39223182-39223232	HCT-116	colon:	n/a
14	chr8:39196907-39196957	HEK293	kidney:	embryo
15	chr8:39196907-39196957	HPAEpiC	pulmonary alveolar:	n/a
16	chr8:39223182-39223232	SK-N-MC	brain:	n/a
17	chr8:39223182-39223232	HRE	kidney:	n/a
18	chr8:39223182-39223232	HCPEpiC	choroid plexus:	n/a
19	chr8:39223182-39223232	MCF10A-Er-Src	breast:	n/a
20	chr8:39196907-39196957	AG04449	skin:	fetal
21	chr8:39223182-39223232	HL-60	blood:	n/a
22	chr8:39223182-39223232	IMR90	lung:	fetal
23	chr8:39196907-39196957	GM12891	blood:	n/a
24	chr8:39223182-39223232	AG09309	skin:	n/a
25	chr8:39196907-39196957	SK-N-SH	brain:	n/a
26	chr8:39196907-39196957	NHBE	bronchial:	n/a
27	chr8:39196907-39196957	HRCEpiC	kidney:	n/a
28	chr8:39196907-39196957	PANC-1	pancreas:	n/a
29	chr8:39196907-39196957	T-47D	breast:	n/a
30	chr8:39196907-39196957	HMEC	breast:	n/a
31	chr8:39196907-39196957	Hela-S3	cervix:	n/a
32	chr8:39196907-39196957	NHDF-neo	bronchial:	n/a
33	chr8:39223182-39223232	Hepatocyte	liver:	n/a
34	chr8:39223182-39223232	AG04450	lung:	fetal
35	chr8:39223182-39223232	HEEpiC	esophagus:	n/a
36	chr8:39196907-39196957	HCT-116	colon:	n/a
37	chr8:39223182-39223232	HRCEpiC	kidney:	n/a
38	chr8:39196907-39196957	PFSK-1	brain:	n/a
39	chr8:39223182-39223232	Caco-2	colon:	n/a
40	chr8:39223182-39223232	HMEC	breast:	n/a
41	chr8:39196907-39196957	GM19239	blood:	n/a
42	chr8:39223182-39223232	K562	blood:	n/a
43	chr8:39196907-39196957	HAEpiC	amniotic membrane:	n/a
44	chr8:39223182-39223232	BE2_C	brain:	n/a
45	chr8:39196907-39196957	HUVEC	blood vessel:	n/a
46	chr8:39196907-39196957	AG04450	lung:	fetal
47	chr8:39223182-39223232	NT2-D1	testis:	n/a
48	chr8:39196907-39196957	SKMC	muscle:	n/a
49	chr8:39196907-39196957	ECC-1	luminal epithelium:	n/a
50	chr8:39196907-39196957	BJ	skin:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:39202201..39204201-chr8:39430573..39432669,2	K562	blood:
2	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
3	chr8:39204717..39207276-chr8:39207847..39209394,2	K562	blood:
4	chr8:38824064..38824622-chr8:39184733..39185545,2	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126157
2	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT147628
3	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT147629
4	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126148
5	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT147628
6	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126152
7	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126148
8	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126153
9	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT126148
10	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126150
11	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126155
12	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126150
13	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126148
14	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT147629
15	lnc-ADAM32-1	chr8:39180489-39181258	NONHSAT126149
16	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126156
17	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126150
18	lnc-ADAM32-1	chr8:39192919-39193008	NONHSAT126156
19	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT147628
20	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT126155
21	lnc-ADAM32-1	chr8:39192919-39193012	NONHSAT126157
22	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126155
23	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126152
24	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126151
25	lnc-ADAM32-1	chr8:39203380-39203563	NONHSAT147628
26	lnc-ADAM32-1	chr8:39233198-39233396	NONHSAT126151
27	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126157
28	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126152
29	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126154
30	lnc-ADAM32-1	chr8:39181687-39181858	NONHSAT126153
31	lnc-ADAM32-1	chr8:39181838-39181858	NONHSAT147629
32	lnc-ADAM32-1	chr8:39182732-39182797	NONHSAT126151

No data

Variant related genes	Relation type
ADAM5	TF binding region
ADAM5	CpG island

Extended variants
information (count: 361 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549522879	chr8:39180899-39180900	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs530697701	chr8:39180912-39180913	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs550524980	chr8:39180930-39180931	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs183845084	chr8:39180937-39180938	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs567989087	chr8:39180976-39180977	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs187760135	chr8:39181018-39181019	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs569163503	chr8:39181093-39181094	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs533469543	chr8:39181221-39181222	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs199577980	chr8:39181242-39181243	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs34525881	chr8:39181256-39181257	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs546521073	chr8:39181697-39181698	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs373331411	chr8:39181731-39181732	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs72580367	chr8:39181738-39181739	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs34280617	chr8:39181739-39181740	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs566515439	chr8:39181742-39181743	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs535808722	chr8:39181745-39181746	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs549132841	chr8:39181757-39181758	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs569288359	chr8:39181793-39181794	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs558751420	chr8:39181796-39181797	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs189976706	chr8:39181798-39181799	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs148347936	chr8:39182760-39182761	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs542823779	chr8:39184069-39184070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192810116	chr8:39184111-39184112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs10104322	chr8:39184151-39184152	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs201536573	chr8:39184175-39184176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs71218324	chr8:39184193-39184194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566706405	chr8:39184217-39184218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs545380321	chr8:39184226-39184227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs77065008	chr8:39184248-39184249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs80024675	chr8:39184282-39184283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs139879416	chr8:39184288-39184289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145331523	chr8:39184302-39184303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs75245319	chr8:39184303-39184304	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs147278271	chr8:39184330-39184331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs569404198	chr8:39184351-39184352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75157358	chr8:39184356-39184357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs60915009	chr8:39184357-39184358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74579930	chr8:39184381-39184382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371305513	chr8:39184482-39184483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149794131	chr8:39184486-39184487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs550374047	chr8:39184498-39184499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs570209855	chr8:39184523-39184524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538958199	chr8:39184575-39184576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554978424	chr8:39184587-39184588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113319257	chr8:39184590-39184591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs557322337	chr8:39184603-39184604	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs570957752	chr8:39184615-39184616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184562956	chr8:39184650-39184651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs566736956	chr8:39184675-39184676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553620781	chr8:39184709-39184710	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	21979893	CNVD
Prostate cancer	16573809	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
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	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
Colorectal cancer	16272173	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
Melanoma	18172304	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
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bladder cancer	19088036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	17001308	CNVD
Breast cancer	17157792	CNVD
Cancer	17001308	CNVD
Cancer	18840272	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Chordoma	18071362	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21785460	CNVD
abnormal development	18461090	CNVD
Breast cancer	16620391	CNVD
Rhabdomyosarcoma	16790082	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21138945	CNVD
Prader-willi syndrome	20588305	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20932292	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:39184000-39187000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr8:39184600-39187000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr8:39184800-39185000	Enhancers	A549	lung
4	chr8:39184800-39185400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr8:39184800-39185400	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr8:39185400-39187200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:39185400-39187400	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:39186800-39187000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr8:39186800-39188000	Enhancers	H9 Cell Line	embryonic stem cell
10	chr8:39187200-39188000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr8:39187200-39188200	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr8:39187400-39188000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr8:39187400-39188200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr8:39187600-39188000	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr8:39188000-39189400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:39188000-39189400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr8:39188200-39189200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr8:39189200-39189800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr8:39189400-39189800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr8:39189400-39189800	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr8:39189600-39190000	Enhancers	Fetal Stomach	stomach
22	chr8:39190200-39191000	Enhancers	Fetal Kidney	kidney
23	chr8:39190400-39191600	Enhancers	Fetal Lung	lung
24	chr8:39191200-39191400	Enhancers	Osteobl	bone
25	chr8:39191200-39191600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr8:39210800-39211400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr8:39215000-39215400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr8:39221000-39222000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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