Variant report

Variant	esv1795075
Chromosome Location	chr8:125692343-125713791
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:125683953..125685840-chr8:125696381..125699279,2	K562	blood:
2	chr8:125662479..125664337-chr8:125697312..125699450,2	MCF-7	breast:
3	chr8:125688216..125690595-chr8:125693629..125695701,2	MCF-7	breast:
4	chr8:125698153..125699926-chr8:125701399..125703514,2	MCF-7	breast:
5	chr8:125709363..125711180-chr8:125714341..125716125,2	K562	blood:
6	chr8:125695412..125697895-chr8:125698374..125700260,3	K562	blood:
7	chr8:125549825..125551523-chr8:125704908..125707139,2	MCF-7	breast:
8	chr8:125692471..125696543-chr8:125697551..125702907,8	MCF-7	breast:
9	chr8:125685458..125688128-chr8:125691791..125694776,4	K562	blood:
10	chr8:125654082..125656755-chr8:125691015..125693469,2	MCF-7	breast:
11	chr8:125691541..125693410-chr8:125699337..125702160,2	K562	blood:
12	chr8:125691541..125693410-chr8:125699337..125702160,2	K562	blood:
13	chr8:125713266..125715229-chr8:125826242..125828033,2	K562	blood:
14	chr8:125681064..125685199-chr8:125693703..125697375,3	MCF-7	breast:
15	chr8:125710245..125712051-chr8:125714540..125716829,2	MCF-7	breast:
16	chr8:125697510..125699727-chr8:125700656..125702402,2	MCF-7	breast:
17	chr8:125692471..125696543-chr8:125697551..125702907,8	MCF-7	breast:
18	chr8:125704431..125707211-chr8:125707702..125710134,3	K562	blood:
19	chr8:125703672..125706290-chr8:125714899..125717654,2	MCF-7	breast:
20	chr8:125597468..125600069-chr8:125711742..125713559,2	MCF-7	breast:
21	chr8:125697915..125700956-chr8:125703472..125706654,3	K562	blood:
22	chr8:125710029..125712501-chr8:125825729..125827888,2	K562	blood:
23	chr8:125700027..125702376-chr8:125709128..125711425,2	K562	blood:
24	chr8:125684155..125685745-chr8:125693552..125695356,2	MCF-7	breast:
25	chr8:125703204..125704827-chr8:125704961..125706579,2	MCF-7	breast:
26	chr8:125700027..125702376-chr8:125709128..125711425,2	K562	blood:
27	chr8:125712421..125715090-chr8:125719227..125721768,2	K562	blood:
28	chr8:125653538..125655457-chr8:125699736..125702279,2	K562	blood:
29	chr8:125707388..125710069-chr8:125729012..125730641,2	MCF-7	breast:
30	chr8:125710219..125712075-chr8:125745092..125746820,2	K562	blood:
31	chr8:125695412..125697895-chr8:125698374..125700260,3	K562	blood:
32	chr8:125706593..125708735-chr8:125715308..125717411,2	MCF-7	breast:
33	chr8:125695281..125696989-chr8:125701339..125704256,2	MCF-7	breast:
34	chr8:125703204..125704827-chr8:125704961..125706579,2	MCF-7	breast:
35	chr8:125695281..125696989-chr8:125701339..125704256,2	MCF-7	breast:
36	chr8:125697510..125699727-chr8:125700656..125702402,2	MCF-7	breast:
37	chr8:125703076..125705336-chr8:125860623..125862726,2	K562	blood:
38	chr8:125704431..125707211-chr8:125707702..125710134,3	K562	blood:
39	chr8:125699774..125701577-chr8:125704384..125706753,2	K562	blood:
40	chr8:125550176..125552813-chr8:125691771..125693317,2	K562	blood:
41	chr8:125699774..125701577-chr8:125704384..125706753,2	K562	blood:
42	chr8:125698153..125699926-chr8:125701399..125703514,2	MCF-7	breast:
43	chr8:125697915..125700956-chr8:125703472..125706654,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000255491	chromatin interactions
ENSG00000147687	chromatin interactions
ENSG00000249816	chromatin interactions
ENSG00000170873	chromatin interactions
ENSG00000147684	chromatin interactions

Extended variants
information (count: 890 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:890 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561415118	chr8:125692369-125692370	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs530296813	chr8:125692440-125692441	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs61433042	chr8:125692497-125692498	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs563747591	chr8:125692498-125692499	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs73345813	chr8:125692535-125692536	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs553108639	chr8:125692536-125692537	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs182813675	chr8:125692558-125692559	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs188813864	chr8:125692583-125692584	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs536237285	chr8:125692586-125692587	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs565632120	chr8:125692631-125692632	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs149280463	chr8:125692637-125692638	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs573179722	chr8:125692643-125692644	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs6984418	chr8:125692664-125692665	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs56218596	chr8:125692690-125692691	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs374003476	chr8:125692705-125692706	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs567531052	chr8:125692751-125692752	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs558903225	chr8:125692791-125692792	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs148783626	chr8:125692807-125692808	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs11778149	chr8:125692861-125692862	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs553033709	chr8:125692891-125692892	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs572468235	chr8:125692898-125692899	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs544782173	chr8:125692900-125692901	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs111284802	chr8:125692921-125692922	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs192919527	chr8:125692970-125692971	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs147959895	chr8:125692982-125692983	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs78432127	chr8:125693056-125693057	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs532608966	chr8:125693114-125693115	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs114768854	chr8:125693118-125693119	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs12677084	chr8:125693155-125693156	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs76160266	chr8:125693180-125693181	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs547814416	chr8:125693187-125693188	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs567733069	chr8:125693198-125693199	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs115466962	chr8:125693219-125693220	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs550406425	chr8:125693227-125693228	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs540787398	chr8:125693235-125693236	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs542639066	chr8:125693273-125693274	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs570585927	chr8:125693324-125693325	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539301852	chr8:125693333-125693334	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs145366189	chr8:125693351-125693352	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147684046	chr8:125693369-125693370	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs536401362	chr8:125693379-125693380	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140980327	chr8:125693395-125693396	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs76232348	chr8:125693462-125693463	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs535765469	chr8:125693500-125693501	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs554977003	chr8:125693501-125693502	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs184692775	chr8:125693529-125693530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189668958	chr8:125693588-125693589	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs150225878	chr8:125693604-125693605	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191277153	chr8:125693651-125693652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs546105744	chr8:125693700-125693701	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:145)

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
Multiple myeloma	17550852	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
Prostate cancer	22341455	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1013 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125673000-125699000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:125676200-125699200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr8:125681200-125701000	Weak transcription	HMEC	breast
4	chr8:125685800-125694600	Weak transcription	Gastric	stomach
5	chr8:125686200-125693000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr8:125686200-125694400	Weak transcription	Pancreas	Pancrea
7	chr8:125686200-125694600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr8:125686200-125695600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr8:125686200-125695800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr8:125686200-125696000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr8:125686200-125697600	Weak transcription	HUVEC	blood vessel
12	chr8:125686200-125699600	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr8:125686400-125692400	Weak transcription	Brain Anterior Caudate	brain
14	chr8:125686400-125694400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr8:125686400-125694400	Weak transcription	Esophagus	oesophagus
16	chr8:125686400-125694800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr8:125686400-125698400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr8:125686400-125698400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr8:125686400-125699400	Weak transcription	Primary T cells from cord blood	blood
20	chr8:125686800-125692600	Weak transcription	Placenta	Placenta
21	chr8:125686800-125692800	Weak transcription	Adipose Nuclei	Adipose
22	chr8:125686800-125694200	Weak transcription	Fetal Brain Female	brain
23	chr8:125686800-125694400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
24	chr8:125686800-125694600	Weak transcription	Fetal Muscle Trunk	muscle
25	chr8:125686800-125699600	Weak transcription	Rectal Mucosa Donor 29	rectum
26	chr8:125687000-125694400	Weak transcription	Fetal Muscle Leg	muscle
27	chr8:125687400-125694400	Weak transcription	Lung	lung
28	chr8:125687600-125694400	Weak transcription	Fetal Thymus	thymus
29	chr8:125687600-125699200	Weak transcription	Fetal Intestine Small	intestine
30	chr8:125687800-125694600	Weak transcription	Spleen	Spleen
31	chr8:125688200-125699600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr8:125689200-125693800	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr8:125689600-125694400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr8:125689600-125694400	Weak transcription	Fetal Lung	lung
35	chr8:125689800-125694600	Weak transcription	Fetal Stomach	stomach
36	chr8:125690000-125692600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
37	chr8:125690000-125692600	Weak transcription	Brain Substantia Nigra	brain
38	chr8:125690000-125692800	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr8:125690000-125693200	Weak transcription	Stomach Smooth Muscle	stomach
40	chr8:125690400-125692400	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr8:125690400-125692600	Weak transcription	Brain Germinal Matrix	brain
42	chr8:125690400-125693400	Weak transcription	Brain Cingulate Gyrus	brain
43	chr8:125690400-125694400	Weak transcription	Brain Angular Gyrus	brain
44	chr8:125690400-125694800	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr8:125690400-125694800	Weak transcription	Colon Smooth Muscle	Colon
46	chr8:125690400-125696600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr8:125690600-125693000	Weak transcription	Brain Hippocampus Middle	brain
48	chr8:125690800-125692400	Strong transcription	Primary B cells from cord blood	blood
49	chr8:125690800-125693200	Enhancers	Left Ventricle	heart
50	chr8:125691200-125693400	Weak transcription	Fetal Brain Male	brain

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