Variant report

Variant	nsv539723
Chromosome Location	chr8:112588983-112711706
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:243)
CpG islands
(count:305)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:243 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr8:112691006-112691050	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr8:112692464-112692870	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr8:112691833-112692033	H1-hESC	embryonic stem cell:	n/a	n/a
4	CBX3	chr8:112678378-112678702	K562	blood:	n/a	n/a
5	CEBPB	chr8:112589943-112590245	HepG2	liver:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
6	CEBPB	chr8:112658465-112658728	MCF-7	breast:	n/a	n/a
7	CEBPB	chr8:112656669-112656973	A549	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
8	CEBPB	chr8:112656695-112656966	IMR90	lung:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
9	CEBPB	chr8:112631993-112632244	HepG2	liver:	n/a	chr8:112632167-112632180
10	CEBPB	chr8:112656674-112657002	HepG2	liver:	n/a	chr8:112656728-112656741 chr8:112656830-112656841
11	CEBPB	chr8:112704205-112704474	HepG2	liver:	n/a	n/a
12	CEBPB	chr8:112589952-112590235	A549	lung:	n/a	chr8:112590133-112590146 chr8:112590111-112590122 chr8:112590110-112590123
13	CEBPB	chr8:112648825-112649214	HepG2	liver:	n/a	chr8:112649115-112649126 chr8:112649115-112649126
14	CEBPB	chr8:112603419-112603617	HepG2	liver:	n/a	chr8:112603525-112603536
15	CEBPB	chr8:112618812-112619060	HepG2	liver:	n/a	chr8:112618953-112618964 chr8:112618955-112618964
16	CEBPB	chr8:112603408-112603661	H1-hESC	embryonic stem cell:	n/a	chr8:112603525-112603536
17	CEBPB	chr8:112711608-112711664	A549	lung:	n/a	chr8:112711627-112711640
18	CHD1	chr8:112693285-112693365	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD2	chr8:112691897-112692838	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTBP2	chr8:112691896-112692704	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr8:112637016-112637365	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr8:112636240-112636390	HepG2	liver:	n/a	n/a
23	CTCF	chr8:112637161-112637213	MCF-7	breast:	n/a	n/a
24	CTCF	chr8:112636259-112636349	MCF-7	breast:	n/a	n/a
25	CTCF	chr8:112625382-112625439	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr8:112636205-112636329	HepG2	liver:	n/a	n/a
27	CTCF	chr8:112636215-112636372	HepG2	liver:	n/a	n/a
28	CTCF	chr8:112636237-112636326	MCF-7	breast:	n/a	n/a
29	CTCF	chr8:112637100-112637250	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr8:112637136-112637227	HepG2	liver:	n/a	n/a
31	CTCF	chr8:112655621-112655698	GM10266	blood:	n/a	n/a
32	CTCF	chr8:112705200-112705350	GM12869	blood:	n/a	n/a
33	CTCF	chr8:112637071-112637273	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr8:112636198-112636256	MCF-7	breast:	n/a	n/a
35	CTCF	chr8:112601706-112601740	GM13976	blood:	n/a	n/a
36	CTCF	chr8:112637220-112637370	MCF-7	breast:	n/a	n/a
37	CTCF	chr8:112636180-112636330	MCF-7	breast:	n/a	n/a
38	CTCF	chr8:112705700-112705850	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr8:112636256-112636258	MCF-7	breast:	n/a	n/a
40	CTCF	chr8:112636220-112636370	MCF-7	breast:	n/a	n/a
41	CTCF	chr8:112637109-112637245	MCF-7	breast:	n/a	n/a
42	CTCF	chr8:112687775-112687822	GM13976	blood:	n/a	n/a
43	CTCF	chr8:112637040-112637190	HEK293	kidney:	n/a	n/a
44	CTCF	chr8:112705800-112705950	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr8:112686779-112686841	GM13976	blood:	n/a	n/a
46	CTCF	chr8:112637080-112637230	HepG2	liver:	n/a	n/a
47	CUX1	chr8:112692842-112692865	GM12878	blood:	n/a	n/a
48	E2F4	chr8:112619113-112619431	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr8:112695062-112695130	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr8:112671424-112671751	MCF10A-Er-Src	breast:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112612368-112612418	MCF-7	breast:	n/a
2	chr8:112636625-112636675	Jurkat	blood:	n/a
3	chr8:112612368-112612418	AG04449	skin:	fetal
4	chr8:112691450-112691500	AG09309	skin:	n/a
5	chr8:112612368-112612418	HCPEpiC	choroid plexus:	n/a
6	chr8:112655155-112655205	IMR90	lung:	fetal
7	chr8:112636613-112636663	CMK	blood:	n/a
8	chr8:112612368-112612418	Hepatocyte	liver:	n/a
9	chr8:112636613-112636663	HRPEpiC	eye:	n/a
10	chr8:112636625-112636675	AG09319	gingival:	n/a
11	chr8:112655155-112655205	NT2-D1	testis:	n/a
12	chr8:112636613-112636663	T-47D	breast:	n/a
13	chr8:112612368-112612418	HMEC	breast:	n/a
14	chr8:112612368-112612418	ovcar-3	ovarian:	n/a
15	chr8:112612368-112612418	BJ	skin:	n/a
16	chr8:112612368-112612418	Jurkat	blood:	n/a
17	chr8:112691450-112691500	HCM	heart:	n/a
18	chr8:112636613-112636663	SKMC	muscle:	n/a
19	chr8:112636625-112636675	ovcar-3	ovarian:	n/a
20	chr8:112691450-112691500	HIPEpiC	eye:	n/a
21	chr8:112655155-112655205	HRE	kidney:	n/a
22	chr8:112636625-112636675	HNPCEpiC	eye:	n/a
23	chr8:112636613-112636663	Hepatocyte	liver:	n/a
24	chr8:112691450-112691500	IMR90	lung:	fetal
25	chr8:112636625-112636675	AoSMC	blood vessel:	n/a
26	chr8:112636625-112636675	HCT-116	colon:	n/a
27	chr8:112612368-112612418	AG09319	gingival:	n/a
28	chr8:112655155-112655205	Caco-2	colon:	n/a
29	chr8:112636613-112636663	HCM	heart:	n/a
30	chr8:112691450-112691500	HRCEpiC	kidney:	n/a
31	chr8:112655155-112655205	MCF10A-Er-Src	breast:	n/a
32	chr8:112655155-112655205	CMK	blood:	n/a
33	chr8:112655155-112655205	PANC-1	pancreas:	n/a
34	chr8:112636625-112636675	NH-A	brain:	n/a
35	chr8:112636613-112636663	NHBE	bronchial:	n/a
36	chr8:112636625-112636675	HRCEpiC	kidney:	n/a
37	chr8:112612368-112612418	GM12891	blood:	n/a
38	chr8:112691450-112691500	AG10803	skin:	n/a
39	chr8:112612368-112612418	BE2_C	brain:	n/a
40	chr8:112636625-112636675	T-47D	breast:	n/a
41	chr8:112691450-112691500	AoSMC	blood vessel:	n/a
42	chr8:112612368-112612418	PrEC	prostate:	n/a
43	chr8:112636625-112636675	K562	blood:	n/a
44	chr8:112612368-112612418	SAEC	small airway:	n/a
45	chr8:112636613-112636663	GM12892	blood:	n/a
46	chr8:112636625-112636675	BE2_C	brain:	n/a
47	chr8:112691450-112691500	SK-N-SH	brain:	n/a
48	chr8:112691450-112691500	HNPCEpiC	eye:	n/a
49	chr8:112691450-112691500	Hela-S3	cervix:	n/a
50	chr8:112655155-112655205	SK-N-SH	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
2	chr8:112690809..112693633-chr8:112697668..112700424,2	K562	blood:
3	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
4	chr8:112706535..112708436-chr8:112710150..112712072,2	K562	blood:
5	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:
6	chr8:112622384..112625093-chr8:112625173..112626907,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CSMD3-4	chr8:112633687-112634026	NONHSAT128329

No data

Variant related genes	Relation type
ENSG00000253156	TF binding region
ENSG00000253156	CpG island

Extended variants
information (count: 1094 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:1094 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572809320	chr8:112593605-112593606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73329965	chr8:112593651-112593652	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558448219	chr8:112593667-112593668	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs187424609	chr8:112593668-112593669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189297209	chr8:112593672-112593673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563418982	chr8:112593674-112593675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12541903	chr8:112593681-112593682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs542448918	chr8:112593708-112593709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs559113387	chr8:112593710-112593711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs180975421	chr8:112593746-112593747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs544904448	chr8:112593749-112593750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs564796555	chr8:112593771-112593772	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs77467730	chr8:112597018-112597019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573285670	chr8:112597027-112597028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs111519293	chr8:112597034-112597035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558803497	chr8:112597040-112597041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs575669122	chr8:112597048-112597049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs544510743	chr8:112597090-112597091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567580993	chr8:112597126-112597127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192989255	chr8:112597213-112597214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140943423	chr8:112597237-112597238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs545015679	chr8:112597280-112597281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs538026576	chr8:112597301-112597302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs150185301	chr8:112597314-112597315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560371929	chr8:112597336-112597337	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76234602	chr8:112597342-112597343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs552129395	chr8:112597350-112597351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565146058	chr8:112597352-112597353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568894270	chr8:112597368-112597369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141069010	chr8:112597370-112597371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144820813	chr8:112597397-112597398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547587427	chr8:112597398-112597399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs138664839	chr8:112597433-112597434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533936526	chr8:112597443-112597444	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs554121881	chr8:112597444-112597445	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369929792	chr8:112597550-112597551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs7013456	chr8:112597601-112597602	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs558892575	chr8:112597699-112597700	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575690331	chr8:112597712-112597713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs544689137	chr8:112597713-112597714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554595136	chr8:112597732-112597733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574700963	chr8:112597755-112597756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540400839	chr8:112597797-112597798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34597469	chr8:112597802-112597803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538740264	chr8:112597808-112597809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs185228871	chr8:112597836-112597837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141667514	chr8:112597866-112597867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs562503767	chr8:112597880-112597881	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531164828	chr8:112597881-112597882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189443049	chr8:112597898-112597899	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112593600-112593800	Enhancers	Pancreas	Pancrea
2	chr8:112597000-112598400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:112611000-112611800	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr8:112611400-112612000	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr8:112611600-112611800	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr8:112611600-112612200	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr8:112611800-112612000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr8:112611800-112612800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
9	chr8:112615400-112615800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr8:112623600-112624000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:112623800-112624200	ZNF genes & repeats	Spleen	Spleen
12	chr8:112624000-112624200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr8:112624000-112624200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
14	chr8:112624000-112627600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr8:112624200-112633800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr8:112627200-112628000	Enhancers	Brain Germinal Matrix	brain
17	chr8:112627600-112628200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr8:112633800-112634000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr8:112633800-112634000	Bivalent Enhancer	Aorta	Aorta
20	chr8:112655000-112655200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:112655200-112655400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr8:112665400-112666000	Enhancers	Fetal Muscle Leg	muscle
23	chr8:112688200-112689400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr8:112688200-112690400	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr8:112689400-112689800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr8:112689600-112690400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr8:112689600-112690400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr8:112689800-112690200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:112690000-112690400	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr8:112690000-112690600	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr8:112690000-112690600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:112690000-112690800	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:112690200-112691400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:112690200-112692200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr8:112690200-112692400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr8:112690200-112694000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr8:112690400-112690600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr8:112690400-112691000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
39	chr8:112690400-112691200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
40	chr8:112690400-112691200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr8:112690400-112691400	Enhancers	H9 Cell Line	embryonic stem cell
42	chr8:112690400-112693400	Enhancers	H1 Cell Line	embryonic stem cell
43	chr8:112690400-112693400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr8:112690600-112691000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr8:112690600-112691200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
46	chr8:112690600-112691200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
47	chr8:112690600-112692200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr8:112690800-112691000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr8:112690800-112691000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr8:112690800-112691400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell

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