Variant report

Variant	nsv528288
Chromosome Location	chr8:125838127-125847357
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:71)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:71 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:125842924-125843329	K562	blood:	n/a	n/a
2	ARID3A	chr8:125840053-125840070	K562	blood:	n/a	n/a
3	ATF1	chr8:125842960-125843264	K562	blood:	n/a	n/a
4	CBX3	chr8:125844467-125844794	K562	blood:	n/a	n/a
5	CCNT2	chr8:125842933-125843212	K562	blood:	n/a	n/a
6	CEBPB	chr8:125846856-125847016	HepG2	liver:	n/a	chr8:125846948-125846959
7	CEBPB	chr8:125842938-125843254	IMR90	lung:	n/a	n/a
8	CEBPB	chr8:125846849-125846993	H1-hESC	embryonic stem cell:	n/a	chr8:125846948-125846959
9	CEBPB	chr8:125846777-125847141	HepG2	liver:	n/a	chr8:125846948-125846959
10	CEBPB	chr8:125846919-125846997	IMR90	lung:	n/a	chr8:125846948-125846959
11	CEBPB	chr8:125842948-125843264	K562	blood:	n/a	n/a
12	CEBPB	chr8:125842914-125843270	K562	blood:	n/a	n/a
13	CTCF	chr8:125845000-125845150	SAEC	small airway:	n/a	n/a
14	CTCF	chr8:125845080-125845230	NHEK	skin:	n/a	n/a
15	CTCF	chr8:125845120-125845270	NHEK	skin:	n/a	n/a
16	CTCF	chr8:125845040-125845190	SAEC	small airway:	n/a	n/a
17	CTCF	chr8:125845120-125845270	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr8:125847276-125847365	HepG2	liver:	n/a	n/a
19	CTCF	chr8:125847240-125847390	HepG2	liver:	n/a	n/a
20	CTCF	chr8:125845080-125845230	HMEC	breast:	n/a	n/a
21	CUX1	chr8:125838619-125838819	K562	blood:	n/a	n/a
22	EP300	chr8:125843054-125843394	K562	blood:	n/a	n/a
23	EP300	chr8:125842910-125843343	K562	blood:	n/a	n/a
24	FOS	chr8:125842913-125843540	HUVEC	blood vessel:	n/a	n/a
25	FOS	chr8:125842906-125843267	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr8:125842912-125843265	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr8:125842928-125843218	MCF10A-Er-Src	breast:	n/a	n/a
28	GATA1	chr8:125842649-125843435	PBDE	blood:	n/a	chr8:125843394-125843405
29	GATA2	chr8:125842834-125843325	K562	blood:	n/a	n/a
30	GATA2	chr8:125842834-125843684	HUVEC	blood vessel:	n/a	chr8:125843556-125843572
31	HDAC2	chr8:125846762-125847125	HepG2	liver:	n/a	chr8:125846979-125846993
32	IRF1	chr8:125842906-125843238	K562	blood:	n/a	n/a
33	JUN	chr8:125842941-125843275	K562	blood:	n/a	n/a
34	JUN	chr8:125842924-125843245	K562	blood:	n/a	n/a
35	JUN	chr8:125838308-125838314	H1-hESC	embryonic stem cell:	n/a	n/a
36	JUND	chr8:125842672-125843299	K562	blood:	n/a	n/a
37	MAFF	chr8:125842867-125843232	K562	blood:	n/a	n/a
38	MAFK	chr8:125842861-125843216	K562	blood:	n/a	n/a
39	MAFK	chr8:125842923-125843149	IMR90	lung:	n/a	n/a
40	MAX	chr8:125846928-125847203	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAX	chr8:125846825-125847251	H1-hESC	embryonic stem cell:	n/a	n/a
42	MAX	chr8:125846912-125847222	HepG2	liver:	n/a	n/a
43	MAZ	chr8:125847211-125847392	HepG2	liver:	n/a	n/a
44	MYC	chr8:125847064-125847118	HepG2	liver:	n/a	n/a
45	MYC	chr8:125842875-125843216	K562	blood:	n/a	n/a
46	MYC	chr8:125840680-125840781	H1-hESC	embryonic stem cell:	n/a	n/a
47	NR2F2	chr8:125842794-125843482	K562	blood:	n/a	n/a
48	NR2F2	chr8:125842921-125843270	K562	blood:	n/a	n/a
49	POLR2A	chr8:125838622-125838724	GM12878	blood:	n/a	n/a
50	RAD21	chr8:125847085-125847489	HepG2	liver:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:125846878..125850160-chr8:125852812..125855632,3	K562	blood:
2	chr8:125838350..125840012-chr8:125843186..125845193,2	MCF-7	breast:
3	chr8:125841473..125844398-chr8:125845586..125849365,3	MCF-7	breast:
4	chr8:125843629..125846063-chr8:125847021..125848938,2	K562	blood:
5	chr8:125825958..125827774-chr8:125846394..125847974,2	K562	blood:
6	chr8:125831862..125834845-chr8:125847342..125849821,2	K562	blood:
7	chr8:125826274..125829204-chr8:125846474..125849665,4	K562	blood:
8	chr8:125845457..125848050-chr8:125858853..125861361,2	MCF-7	breast:
9	chr8:125826707..125829415-chr8:125838382..125840069,3	MCF-7	breast:
10	chr8:125825994..125828112-chr8:125845201..125847041,2	MCF-7	breast:
11	chr8:125832057..125834000-chr8:125846530..125849480,2	MCF-7	breast:
12	chr8:125835660..125838379-chr8:125840194..125843093,3	K562	blood:
13	chr8:125844772..125847545-chr8:125849110..125851069,2	K562	blood:
14	chr8:125835196..125838100-chr8:125838593..125841360,2	K562	blood:
15	chr8:125553598..125555857-chr8:125845725..125847345,2	K562	blood:
16	chr8:125841473..125844398-chr8:125845586..125849365,3	MCF-7	breast:
17	chr8:125838350..125840012-chr8:125843186..125845193,2	MCF-7	breast:
18	chr8:125796943..125799236-chr8:125835444..125838283,2	MCF-7	breast:
19	chr8:125845588..125849228-chr8:125849730..125853632,5	MCF-7	breast:
20	chr8:125847137..125849263-chr8:125851219..125853142,2	K562	blood:
21	chr8:125835660..125838379-chr8:125840194..125843093,3	K562	blood:
22	chr8:125843629..125846063-chr8:125847021..125848938,2	K562	blood:

No data

Variant related genes	Relation type
MIR4662B	TF binding region
ENSG00000147684	chromatin interactions
ENSG00000255491	chromatin interactions
ENSG00000263735	chromatin interactions
ENSG00000249816	chromatin interactions

Extended variants
information (count: 334 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:334 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10098746	chr8:125838127-125838128	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs371023979	chr8:125838154-125838155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs532310182	chr8:125838160-125838161	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541357480	chr8:125838161-125838162	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80346966	chr8:125838168-125838169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs115051114	chr8:125838190-125838191	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189343533	chr8:125838236-125838237	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs139427089	chr8:125838246-125838247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs180939886	chr8:125838344-125838345	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs149977592	chr8:125838363-125838364	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs552296916	chr8:125838365-125838366	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs115860049	chr8:125838375-125838376	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs528274353	chr8:125838403-125838404	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs548526333	chr8:125838420-125838421	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs186192563	chr8:125838450-125838451	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145219729	chr8:125838463-125838464	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs550105060	chr8:125838502-125838503	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs56225987	chr8:125838536-125838537	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs148278262	chr8:125838538-125838539	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538790977	chr8:125838544-125838545	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7462735	chr8:125838550-125838551	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs563772000	chr8:125838560-125838561	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs536713313	chr8:125838565-125838566	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs57223956	chr8:125838566-125838567	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs182869265	chr8:125838610-125838611	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543053472	chr8:125838680-125838681	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs563343082	chr8:125838693-125838694	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs13279419	chr8:125838746-125838747	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs545954419	chr8:125838747-125838748	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs149162167	chr8:125838783-125838784	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186766758	chr8:125838784-125838785	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs144731714	chr8:125838943-125838944	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs561838470	chr8:125838963-125838964	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs370808112	chr8:125838990-125838991	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373896329	chr8:125839018-125839019	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs530884808	chr8:125839030-125839031	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs550594358	chr8:125839031-125839032	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147812176	chr8:125839033-125839034	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191606490	chr8:125839048-125839049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549265530	chr8:125839073-125839074	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs10087607	chr8:125839079-125839080	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs552273812	chr8:125839087-125839088	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs111508679	chr8:125839112-125839113	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs534894567	chr8:125839254-125839255	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73349141	chr8:125839275-125839276	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs183168267	chr8:125839360-125839361	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs7005642	chr8:125839368-125839369	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs557354320	chr8:125839375-125839376	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs4871555	chr8:125839379-125839380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs75598469	chr8:125839425-125839426	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
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
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	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
Acute myeloid leukemia	20729466	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
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	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
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Gastric cancer	18160780	CNVD

Chromatin state (count:166 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125836400-125838400	Weak transcription	Fetal Muscle Leg	muscle
2	chr8:125836400-125838600	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr8:125836400-125839200	Weak transcription	Spleen	Spleen
4	chr8:125836400-125839800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr8:125836400-125841400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr8:125836400-125850800	Weak transcription	Right Atrium	heart
7	chr8:125836600-125841800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr8:125836800-125842000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:125836800-125843200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr8:125837200-125838600	Enhancers	Monocytes-CD14+_RO01746	blood
11	chr8:125837600-125838400	Enhancers	K562	blood
12	chr8:125837800-125838200	Enhancers	NHDF-Ad	bronchial
13	chr8:125838000-125842200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:125838200-125843000	Weak transcription	NHDF-Ad	bronchial
15	chr8:125838400-125838600	Enhancers	Fetal Muscle Leg	muscle
16	chr8:125838400-125840800	Weak transcription	K562	blood
17	chr8:125839200-125839400	Enhancers	Spleen	Spleen
18	chr8:125839400-125839600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr8:125839800-125840200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr8:125839800-125842600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr8:125840000-125841000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr8:125840200-125842000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr8:125840800-125844000	Enhancers	K562	blood
24	chr8:125841000-125841400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr8:125841000-125842400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr8:125841200-125844000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr8:125841400-125841600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr8:125841400-125842400	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr8:125841600-125843200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr8:125841800-125842400	Enhancers	Skeletal Muscle Male	skeletal muscle
31	chr8:125842000-125842200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
32	chr8:125842000-125842400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:125842000-125844000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr8:125842200-125842400	Enhancers	Esophagus	oesophagus
35	chr8:125842200-125843200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr8:125842200-125843600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr8:125842200-125843800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:125842200-125843800	Enhancers	HUVEC	blood vessel
39	chr8:125842200-125843800	Enhancers	Osteobl	bone
40	chr8:125842200-125844800	Weak transcription	Psoas Muscle	Psoas
41	chr8:125842200-125845600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr8:125842400-125843600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr8:125842400-125844000	Enhancers	Stomach Mucosa	stomach
44	chr8:125842400-125844600	Weak transcription	Esophagus	oesophagus
45	chr8:125842400-125845800	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr8:125842400-125846600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr8:125842400-125846600	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr8:125842600-125843400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr8:125843000-125843200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr8:125843000-125844000	Enhancers	Hela-S3	cervix

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