Variant report

Variant	esv994614
Chromosome Location	chr8:67524820-67525293
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	chr8:67524810-67524926	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCLAF1	chr8:67525268-67526349	GM12878	blood:	n/a	chr8:67525271-67525284 chr8:67526292-67526301 chr8:67525966-67525974
3	BHLHE40	chr8:67524986-67526385	K562	blood:	n/a	n/a
4	BRCA1	chr8:67524761-67525287	H1-hESC	embryonic stem cell:	n/a	n/a
5	BRCA1	chr8:67524814-67524845	GM12878	blood:	n/a	n/a
6	BRCA1	chr8:67525144-67525203	Hela-S3	cervix:	n/a	n/a
7	CCNT2	chr8:67524954-67526028	K562	blood:	n/a	chr8:67525260-67525269
8	CEBPD	chr8:67525249-67526016	HepG2	liver:	n/a	n/a
9	CHD1	chr8:67525124-67525336	H1-hESC	embryonic stem cell:	n/a	n/a
10	CHD2	chr8:67525034-67526348	HepG2	liver:	n/a	n/a
11	CHD2	chr8:67524988-67525117	K562	blood:	n/a	n/a
12	CHD2	chr8:67524965-67526190	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr8:67524677-67526566	Hela-S3	cervix:	n/a	n/a
14	CREB1	chr8:67525267-67526080	GM12878	blood:	n/a	n/a
15	CREB1	chr8:67525024-67526005	HepG2	liver:	n/a	n/a
16	CREB1	chr8:67525272-67526013	K562	blood:	n/a	n/a
17	CREB1	chr8:67525020-67525949	H1-hESC	embryonic stem cell:	n/a	n/a
18	CREB1	chr8:67524801-67526492	HepG2	liver:	n/a	n/a
19	CREB1	chr8:67525034-67526013	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr8:67525002-67526094	A549	lung:	n/a	n/a
21	CTBP2	chr8:67524683-67525929	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr8:67525140-67525290	HepG2	liver:	n/a	chr8:67525174-67525192
23	CTCF	chr8:67525020-67525170	SK-N-SH_RA	brain:	n/a	chr8:67525123-67525136
24	CTCF	chr8:67525100-67525250	SAEC	small airway:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
25	CTCF	chr8:67525080-67525230	AG04450	lung:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
26	CTCF	chr8:67525060-67525210	BE2_C	brain:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
27	CTCF	chr8:67525220-67525370	GM12869	blood:	n/a	n/a
28	CTCF	chr8:67525100-67525250	HCFaa	heart:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
29	CTCF	chr8:67524760-67524910	AoAF	blood vessel:	n/a	n/a
30	CTCF	chr8:67525000-67525150	GM12875	blood:	n/a	chr8:67525123-67525136
31	CTCF	chr8:67525060-67525210	HMEC	breast:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
32	CTCF	chr8:67525160-67525310	GM12871	blood:	n/a	chr8:67525174-67525192
33	CTCF	chr8:67525080-67525230	HUVEC	blood vessel:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
34	CTCF	chr8:67525080-67525230	HPAF	blood vessel:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
35	CTCF	chr8:67525020-67525170	MCF-7	breast:	n/a	chr8:67525123-67525136
36	CTCF	chr8:67525060-67525210	HRE	kidney:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
37	CTCF	chr8:67525080-67525230	HBMEC	blood vessel:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
38	CTCF	chr8:67525140-67525290	HMEC	breast:	n/a	chr8:67525174-67525192
39	CTCF	chr8:67525080-67525230	WERI-Rb-1	eye:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
40	CTCF	chr8:67525053-67525916	K562	blood:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
41	CTCF	chr8:67525197-67525208	GM19239	blood:	n/a	n/a
42	CTCF	chr8:67525160-67525310	GM12865	blood:	n/a	chr8:67525174-67525192
43	CTCF	chr8:67525065-67525251	A549	lung:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
44	CTCF	chr8:67525060-67525210	HEK293	kidney:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
45	CTCF	chr8:67525120-67525270	HEK293	kidney:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
46	CTCF	chr8:67525080-67525230	HCPEpiC	choroid plexus:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
47	CTCF	chr8:67525200-67525350	HAc	cerebellar:	n/a	n/a
48	CTCF	chr8:67525094-67525930	GM12878	blood:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
49	CTCF	chr8:67525064-67525314	MCF-7	breast:	n/a	chr8:67525174-67525192 chr8:67525123-67525136
50	CTCF	chr8:67524840-67524990	AG09319	gingival:	n/a	chr8:67524973-67524986

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:67525279-67525329	HCPEpiC	choroid plexus:	n/a
2	chr8:67525279-67525329	HCF	heart:	n/a
3	chr8:67525279-67525329	SK-N-MC	brain:	n/a
4	chr8:67525279-67525329	PFSK-1	brain:	n/a
5	chr8:67525279-67525329	HUVEC	blood vessel:	n/a
6	chr8:67525279-67525329	HRE	kidney:	n/a
7	chr8:67525279-67525329	AG09309	skin:	n/a
8	chr8:67525279-67525329	CMK	blood:	n/a
9	chr8:67525279-67525329	HCM	heart:	n/a
10	chr8:67525279-67525329	LNCaP	prostate:	n/a
11	chr8:67525279-67525329	NHBE	bronchial:	n/a
12	chr8:67525279-67525329	BJ	skin:	n/a
13	chr8:67525279-67525329	ECC-1	luminal epithelium:	n/a
14	chr8:67525279-67525329	NB4	blood:	n/a
15	chr8:67525279-67525329	T-47D	breast:	n/a
16	chr8:67525279-67525329	GM19239	blood:	n/a
17	chr8:67525279-67525329	A549	lung:	n/a
18	chr8:67525279-67525329	HEK293	kidney:	embryo
19	chr8:67525279-67525329	HPAEpiC	pulmonary alveolar:	n/a
20	chr8:67525279-67525329	ProgFib	skin:	n/a
21	chr8:67525279-67525329	ovcar-3	ovarian:	n/a
22	chr8:67525279-67525329	Hela-S3	cervix:	n/a
23	chr8:67525279-67525329	HL-60	blood:	n/a
24	chr8:67525279-67525329	PANC-1	pancreas:	n/a
25	chr8:67525279-67525329	GM12878	blood:	n/a
26	chr8:67525279-67525329	Jurkat	blood:	n/a
27	chr8:67525279-67525329	HRCEpiC	kidney:	n/a
28	chr8:67525279-67525329	Caco-2	colon:	n/a
29	chr8:67525279-67525329	AG10803	skin:	n/a
30	chr8:67525279-67525329	NHDF-neo	bronchial:	n/a
31	chr8:67525279-67525329	HRPEpiC	eye:	n/a
32	chr8:67525279-67525329	NH-A	brain:	n/a
33	chr8:67525279-67525329	H1-hESC	embryonic stem cell:	embryo
34	chr8:67525279-67525329	BE2_C	brain:	n/a
35	chr8:67525279-67525329	MCF-7	breast:	n/a
36	chr8:67525279-67525329	HCT-116	colon:	n/a
37	chr8:67525279-67525329	K562	blood:	n/a
38	chr8:67525279-67525329	SKMC	muscle:	n/a
39	chr8:67525279-67525329	U87	brain:	n/a
40	chr8:67525279-67525329	HepG2	liver:	n/a
41	chr8:67525279-67525329	AoSMC	blood vessel:	n/a
42	chr8:67525279-67525329	PrEC	prostate:	n/a
43	chr8:67525279-67525329	NT2-D1	testis:	n/a
44	chr8:67525279-67525329	SK-N-SH_RA	brain:	n/a
45	chr8:67525279-67525329	HMEC	breast:	n/a
46	chr8:67525279-67525329	AG04449	skin:	fetal
47	chr8:67525279-67525329	AG09319	gingival:	n/a
48	chr8:67525279-67525329	MCF10A-Er-Src	breast:	n/a
49	chr8:67525279-67525329	IMR90	lung:	fetal
50	chr8:67525279-67525329	GM12891	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:67523268..67525543-chr8:67973888..67976833,2	MCF-7	breast:
2	chr8:67521707..67525650-chr8:67623825..67627698,8	MCF-7	breast:
3	chr8:67371423..67376205-chr8:67520601..67527002,8	MCF-7	breast:
4	chr8:67341571..67344891-chr8:67522913..67526545,3	MCF-7	breast:
5	chr8:67524115..67526215-chr8:67685855..67687886,2	K562	blood:
6	chr8:67524099..67528801-chr8:67579151..67581449,5	K562	blood:
7	chr8:67523934..67528477-chr8:67576797..67579768,6	MCF-7	breast:
8	chr12:110718828..110719502-chr8:67524980..67525790,2	HCT-116	colon:
9	chr8:67523974..67528801-chr8:67579151..67581998,7	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYBL1-2	chr8:67524926-67525427	NONHSAT127037
2	lnc-MYBL1-2	chr8:67524380-67526482	NONHSAT127036

Variant related genes	Relation type
MYBL1	TF binding region
MYBL1	CpG island
ENSG00000174437	chromatin interactions
ENSG00000169085	chromatin interactions
ENSG00000104218	chromatin interactions
ENSG00000213865	chromatin interactions
ENSG00000270024	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000147576	chromatin interactions
ENSG00000104205	chromatin interactions
ENSG00000175073	chromatin interactions

Extended variants
information (count: 25 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13255518	chr8:67524849-67524850	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	Chromatin interactive region lncRNA	8 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532346756	chr8:67524871-67524872	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
3	rs552483317	chr8:67524902-67524903	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
4	rs72652790	chr8:67524909-67524910	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs576512211	chr8:67524922-67524923	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
6	rs528486939	chr8:67524932-67524933	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
7	rs542209572	chr8:67524933-67524934	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
8	rs184732313	chr8:67524949-67524950	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	9 gene(s)	Overlapped CNVs	n/a
9	rs376214846	chr8:67524987-67524988	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
10	rs568231321	chr8:67524989-67524990	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
11	rs537181966	chr8:67524993-67524994	Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Enhancers	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
12	rs141009728	chr8:67525012-67525013	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
13	rs377298520	chr8:67525017-67525018	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
14	rs570752710	chr8:67525019-67525020	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
15	rs368446250	chr8:67525027-67525028	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
16	rs371855803	chr8:67525059-67525060	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
17	rs376507793	chr8:67525074-67525075	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
18	rs369185230	chr8:67525094-67525095	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
19	rs539605254	chr8:67525097-67525098	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
20	rs146585703	chr8:67525173-67525174	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
21	rs553633094	chr8:67525218-67525219	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
22	rs371447044	chr8:67525228-67525229	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
23	rs534631452	chr8:67525254-67525255	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
24	rs554306115	chr8:67525268-67525269	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a
25	rs376661600	chr8:67525280-67525281	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67522200-67526200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
2	chr8:67522200-67526400	Active TSS	Primary T helper naive cells from peripheral blood	blood
3	chr8:67522600-67527000	Active TSS	NHLF	lung
4	chr8:67522800-67526400	Active TSS	Primary T killer memory cells from peripheral blood	blood
5	chr8:67523200-67526400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr8:67523200-67526600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:67523200-67526600	Active TSS	HSMM	muscle
8	chr8:67523400-67526400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr8:67523600-67525000	Flanking Active TSS	Dnd41	blood
10	chr8:67523600-67525200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr8:67523600-67525200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
12	chr8:67523600-67526200	Active TSS	NH-A	brain
13	chr8:67523600-67526800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr8:67523800-67525000	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:67523800-67525000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr8:67523800-67526200	Active TSS	Brain Germinal Matrix	brain
17	chr8:67523800-67527000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr8:67524000-67525000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr8:67524000-67526200	Active TSS	Primary T killer naive cells fromperipheralblood	blood
20	chr8:67524000-67526400	Active TSS	HMEC	breast
21	chr8:67524000-67526800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr8:67524200-67525000	Flanking Bivalent TSS/Enh	Fetal Lung	lung
23	chr8:67524200-67525000	Flanking Active TSS	HUVEC	blood vessel
24	chr8:67524200-67526400	Active TSS	Breast Myoepithelial Primary Cells	Breast
25	chr8:67524200-67526400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr8:67524200-67526800	Active TSS	H1 Cell Line	embryonic stem cell
27	chr8:67524200-67526800	Active TSS	H9 Cell Line	embryonic stem cell
28	chr8:67524200-67526800	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
29	chr8:67524200-67526800	Active TSS	NHDF-Ad	bronchial
30	chr8:67524200-67527000	Active TSS	A549	lung
31	chr8:67524400-67525000	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
32	chr8:67524400-67525000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:67524400-67525000	Flanking Active TSS	Brain Hippocampus Middle	brain
34	chr8:67524400-67525000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
35	chr8:67524400-67525000	Enhancers	Stomach Mucosa	stomach
36	chr8:67524400-67525200	Flanking Bivalent TSS/Enh	Primary neutrophils fromperipheralblood	blood
37	chr8:67524400-67525200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
38	chr8:67524400-67525200	Flanking Active TSS	Fetal Muscle Leg	muscle
39	chr8:67524400-67525400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr8:67524400-67525400	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
41	chr8:67524400-67525800	Active TSS	HepG2	liver
42	chr8:67524400-67526200	Active TSS	HUES48 Cell Line	embryonic stem cell
43	chr8:67524400-67526400	Active TSS	Muscle Satellite Cultured Cells	--
44	chr8:67524400-67526400	Active TSS	Fetal Kidney	kidney
45	chr8:67524400-67526600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr8:67524400-67526600	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr8:67524400-67526600	Active TSS	HSMMtube	muscle
48	chr8:67524400-67526800	Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chr8:67524400-67526800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr8:67524600-67525000	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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