Variant report

Variant	nsv968490
Chromosome Location	chr8:9088295-9093258
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	BHLHE40	chr8:9090326-9090623	K562	blood:	n/a	n/a
2	CEBPB	chr8:9092228-9092358	K562	blood:	n/a	n/a
3	CEBPB	chr8:9088688-9088983	K562	blood:	n/a	chr8:9088845-9088853 chr8:9088871-9088879
4	CEBPB	chr8:9090364-9090709	K562	blood:	n/a	n/a
5	E2F6	chr8:9088864-9089206	H1-hESC	embryonic stem cell:	n/a	chr8:9088870-9088879
6	EP300	chr8:9089983-9090645	K562	blood:	n/a	chr8:9090410-9090419 chr8:9090145-9090155 chr8:9090280-9090294
7	EP300	chr8:9091012-9091033	K562	blood:	n/a	n/a
8	FAM48A	chr8:9088558-9088670	GM12878	blood:	n/a	n/a
9	IRF1	chr8:9092028-9092059	K562	blood:	n/a	n/a
10	JUND	chr8:9090305-9090666	K562	blood:	n/a	n/a
11	MAFK	chr8:9093109-9093188	IMR90	lung:	n/a	n/a
12	MAX	chr8:9090155-9090548	K562	blood:	n/a	n/a
13	MAX	chr8:9090128-9090537	NB4	blood:	n/a	n/a
14	MYC	chr8:9088533-9088586	K562	blood:	n/a	n/a
15	MYC	chr8:9091902-9091975	H1-hESC	embryonic stem cell:	n/a	n/a
16	NFYA	chr8:9088653-9088989	K562	blood:	n/a	chr8:9088867-9088879 chr8:9088921-9088939 chr8:9088841-9088856 chr8:9088868-9088883 chr8:9088841-9088856 chr8:9088844-9088854 chr8:9088868-9088883 chr8:9088868-9088882 chr8:9088844-9088854 chr8:9088868-9088881 chr8:9088842-9088856 chr8:9088870-9088880 chr8:9088843-9088856 chr8:9088845-9088857
17	NFYB	chr8:9088703-9089072	K562	blood:	n/a	chr8:9088867-9088879 chr8:9088841-9088856 chr8:9088868-9088883 chr8:9088841-9088856 chr8:9088844-9088854 chr8:9088868-9088883 chr8:9088868-9088882 chr8:9088844-9088854 chr8:9088868-9088881 chr8:9088842-9088856 chr8:9088870-9088880 chr8:9088843-9088856 chr8:9088845-9088857
18	SPI1	chr8:9090214-9090639	HL-60	blood:	n/a	chr8:9090410-9090419 chr8:9090407-9090420 chr8:9090408-9090421 chr8:9090411-9090418
19	SPI1	chr8:9090269-9090479	K562	blood:	n/a	chr8:9090410-9090419 chr8:9090407-9090420 chr8:9090408-9090421 chr8:9090411-9090418
20	SPI1	chr8:9090327-9090498	K562	blood:	n/a	chr8:9090410-9090419 chr8:9090407-9090420 chr8:9090408-9090421 chr8:9090411-9090418
21	TEAD4	chr8:9089970-9090711	K562	blood:	n/a	n/a
22	YY1	chr8:9090392-9090609	K562	blood:	n/a	chr8:9090520-9090530 chr8:9090519-9090527
23	ZNF143	chr8:9090290-9090490	K562	blood:	n/a	n/a
24	ZNF274	chr8:9090102-9090563	NT2-D1	testis:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:9090534..9092903-chr8:9095758..9098005,2	MCF-7	breast:
2	chr8:9056772..9059082-chr8:9087003..9089013,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-10A14.4.1-5	chr8:9090523-9090959	NONHSAT124932
2	lnc-RP11-10A14.4.1-6	chr8:9088317-9088952	l_3543_chr8:9084119-9097777_placenta

Variant related genes	Relation type
ENSG00000254091	TF binding region

Extended variants
information (count: 228 )
Associated
traits (count: 135 )

Variant overlapped rSNPs/rCNVs (count:228 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555363983	chr8:9088327-9088328	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
2	rs330055	chr8:9088336-9088337	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540269666	chr8:9088354-9088355	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs567835742	chr8:9088390-9088391	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs138218296	chr8:9088416-9088417	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs192022310	chr8:9088427-9088428	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs185390980	chr8:9088432-9088433	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs35841195	chr8:9088460-9088461	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
9	rs562790198	chr8:9088463-9088464	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
10	rs76913570	chr8:9088470-9088471	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
11	rs74432210	chr8:9088472-9088473	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
12	rs142734803	chr8:9088477-9088478	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
13	rs562249432	chr8:9088518-9088519	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
14	rs34900446	chr8:9088525-9088526	Weak transcription Enhancers Active TSS Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
15	rs527959676	chr8:9088536-9088537	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs547090541	chr8:9088538-9088539	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs564053980	chr8:9088546-9088547	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs55940651	chr8:9088555-9088556	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs533085781	chr8:9088583-9088584	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
20	rs571391161	chr8:9088608-9088609	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
21	rs111718058	chr8:9088624-9088625	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs184133509	chr8:9088633-9088634	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs188288591	chr8:9088658-9088659	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs79678700	chr8:9088717-9088718	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs75173646	chr8:9088726-9088727	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs150170957	chr8:9088756-9088757	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs534903567	chr8:9088773-9088774	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs553779756	chr8:9088775-9088776	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs576824766	chr8:9088780-9088781	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
30	rs35851791	chr8:9088791-9088792	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
31	rs539585542	chr8:9088826-9088827	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
32	rs577424932	chr8:9088858-9088859	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
33	rs181840847	chr8:9088864-9088865	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
34	rs542081751	chr8:9088883-9088884	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
35	rs562277245	chr8:9088909-9088910	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
36	rs6601293	chr8:9088951-9088952	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs541688034	chr8:9088967-9088968	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs186496534	chr8:9088969-9088970	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs532947754	chr8:9088977-9088978	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs138635726	chr8:9088989-9088990	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs375245244	chr8:9089011-9089012	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs149304763	chr8:9089017-9089018	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs116922459	chr8:9089032-9089033	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs189609926	chr8:9089066-9089067	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs565845760	chr8:9089072-9089073	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs113876965	chr8:9089102-9089103	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs575283780	chr8:9089103-9089104	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs551254321	chr8:9089112-9089113	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs181656579	chr8:9089137-9089138	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs372625646	chr8:9089146-9089147	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:135)

Disease	PMID	Source
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
Prostate cancer	16573809	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
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	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
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Bladder cancer	21909424	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:9082800-9088600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr8:9083200-9090200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr8:9087800-9089000	Active TSS	Fetal Brain Female	brain
4	chr8:9088000-9088400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr8:9088000-9088400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr8:9088000-9088400	Active TSS	Aorta	Aorta
7	chr8:9088000-9088400	Flanking Active TSS	Brain Hippocampus Middle	brain
8	chr8:9088000-9088600	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr8:9088000-9088600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
10	chr8:9088000-9088800	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr8:9088000-9088800	Active TSS	Brain Anterior Caudate	brain
12	chr8:9088000-9089200	Active TSS	Brain Angular Gyrus	brain
13	chr8:9088200-9088400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr8:9088200-9088400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
15	chr8:9088200-9088400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
16	chr8:9088200-9088400	Flanking Active TSS	NH-A	brain
17	chr8:9088200-9088800	Active TSS	Brain Substantia Nigra	brain
18	chr8:9088200-9089000	Active TSS	Fetal Brain Male	brain
19	chr8:9088400-9088600	Weak transcription	Aorta	Aorta
20	chr8:9088400-9088600	Active TSS	Brain Inferior Temporal Lobe	brain
21	chr8:9088400-9088800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr8:9088400-9088800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr8:9088400-9088800	Active TSS	Brain Hippocampus Middle	brain
24	chr8:9088400-9088800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr8:9088400-9088800	Active TSS	NH-A	brain
26	chr8:9088600-9088800	Active TSS	Skeletal Muscle Female	skeletal muscle
27	chr8:9088600-9089000	Flanking Active TSS	Brain Cingulate Gyrus	brain
28	chr8:9088600-9089200	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr8:9088600-9089200	Enhancers	Aorta	Aorta
30	chr8:9088600-9089200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
31	chr8:9088800-9089000	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr8:9088800-9089200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr8:9088800-9089200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr8:9088800-9089200	Flanking Active TSS	Brain Anterior Caudate	brain
35	chr8:9088800-9089200	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr8:9088800-9089200	Flanking Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
37	chr8:9088800-9089200	Flanking Active TSS	Brain Substantia Nigra	brain
38	chr8:9088800-9089200	Enhancers	Psoas Muscle	Psoas
39	chr8:9088800-9089200	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr8:9088800-9089200	Enhancers	Thymus	Thymus
41	chr8:9088800-9089400	Enhancers	Dnd41	blood
42	chr8:9089000-9089200	Enhancers	Brain Cingulate Gyrus	brain
43	chr8:9089000-9089200	Flanking Active TSS	Fetal Brain Male	brain
44	chr8:9089000-9089200	Flanking Active TSS	Fetal Brain Female	brain
45	chr8:9089000-9089200	Enhancers	Right Atrium	heart
46	chr8:9089000-9089200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
47	chr8:9089000-9089200	Bivalent Enhancer	HSMMtube	muscle
48	chr8:9089000-9090800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr8:9089200-9089400	Enhancers	Fetal Brain Female	brain
50	chr8:9089200-9090200	Weak transcription	Thymus	Thymus

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