Variant report

Variant	esv275526
Chromosome Location	chr8:125640964-125650653
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:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:125640733..125644991-chr8:125647355..125650506,7	K562	blood:
2	chr8:125631062..125635661-chr8:125637990..125641115,5	MCF-7	breast:
3	chr8:125640493..125643874-chr8:125825913..125829115,5	K562	blood:
4	chr8:125644080..125646951-chr8:125648731..125650374,2	MCF-7	breast:
5	chr8:125617959..125620895-chr8:125642902..125645461,3	MCF-7	breast:
6	chr8:125647545..125651264-chr8:125826076..125829178,3	K562	blood:
7	chr8:125642013..125645236-chr8:125863862..125867426,3	MCF-7	breast:
8	chr8:125639696..125643717-chr8:125738373..125742110,6	MCF-7	breast:
9	chr8:125624893..125627739-chr8:125639327..125643495,3	MCF-7	breast:
10	chr8:125650533..125653150-chr8:125663806..125665478,2	MCF-7	breast:
11	chr8:125638629..125643985-chr8:125739070..125743029,6	MCF-7	breast:
12	chr8:125627308..125630217-chr8:125638327..125642424,3	K562	blood:
13	chr8:125649883..125652177-chr8:125661816..125663375,2	K562	blood:
14	chr8:125640310..125641819-chr8:125649857..125651732,2	MCF-7	breast:
15	chr8:125590632..125592383-chr8:125646702..125648636,2	K562	blood:
16	chr8:125627353..125628937-chr8:125644773..125647709,2	K562	blood:
17	chr8:125603731..125605480-chr8:125649123..125652014,2	K562	blood:
18	chr8:125640310..125641819-chr8:125649857..125651732,2	MCF-7	breast:
19	chr8:125649100..125650648-chr8:125660221..125663028,2	K562	blood:
20	chr8:125625162..125628141-chr8:125641706..125644000,2	MCF-7	breast:
21	chr8:125642370..125644650-chr8:125657174..125658829,2	K562	blood:
22	chr8:125647615..125650010-chr8:125670144..125672819,2	MCF-7	breast:
23	chr8:125639927..125641909-chr8:125654623..125657042,2	MCF-7	breast:
24	chr8:125638351..125644610-chr8:125826258..125829486,6	K562	blood:
25	chr8:125605311..125606257-chr8:125646877..125647660,2	MCF-7	breast:
26	chr8:125630930..125633554-chr8:125639086..125641953,3	K562	blood:
27	chr8:125644080..125646951-chr8:125648731..125650374,2	MCF-7	breast:
28	chr8:125633578..125635485-chr8:125639312..125641576,2	K562	blood:
29	chr8:125640852..125644024-chr8:125644604..125648826,4	MCF-7	breast:
30	chr8:125646525..125649000-chr8:125654557..125656229,2	K562	blood:
31	chr8:125621598..125623778-chr8:125643368..125646296,3	K562	blood:
32	chr8:125647571..125649356-chr8:125735665..125737482,2	MCF-7	breast:
33	chr8:125640852..125644024-chr8:125644604..125648826,4	MCF-7	breast:
34	chr8:125640772..125642364-chr8:125869019..125870864,2	MCF-7	breast:
35	chr8:125647705..125651624-chr8:125656720..125658741,4	K562	blood:
36	chr8:125628873..125632428-chr8:125641301..125644055,3	MCF-7	breast:
37	chr8:125640733..125644991-chr8:125647355..125650506,7	K562	blood:
38	chr8:125648425..125652159-chr8:125652603..125655556,5	K562	blood:
39	chr8:125549859..125552805-chr8:125642129..125643767,2	MCF-7	breast:
40	chr8:125628680..125631257-chr8:125639768..125642424,2	K562	blood:
41	chr8:125648736..125650497-chr8:125657454..125659913,2	MCF-7	breast:
42	chr8:125648801..125651687-chr8:125651691..125654653,2	MCF-7	breast:
43	chr8:125649125..125655229-chr8:125655458..125659458,6	K562	blood:
44	chr8:125636094..125637667-chr8:125641302..125642987,2	MCF-7	breast:
45	chr8:125638065..125640378-chr8:125640492..125642045,2	K562	blood:
46	chr8:125639634..125641843-chr8:125985419..125987948,2	MCF-7	breast:
47	chr8:125643150..125645424-chr8:125657174..125658686,2	K562	blood:
48	chr8:125645660..125649648-chr8:125667642..125669195,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000180938	chromatin interactions
ENSG00000255080	chromatin interactions
ENSG00000255491	chromatin interactions
ENSG00000272486	chromatin interactions
ENSG00000170873	chromatin interactions
ENSG00000147684	chromatin interactions
ENSG00000147687	chromatin interactions

Extended variants
information (count: 392 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4870915	chr8:125640964-125640965	Weak transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs117958680	chr8:125641004-125641005	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs185223294	chr8:125641077-125641078	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs113473758	chr8:125641083-125641084	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs192893929	chr8:125641103-125641104	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs532444710	chr8:125641182-125641183	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs74326025	chr8:125641200-125641201	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs35014080	chr8:125641210-125641211	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs140687540	chr8:125641232-125641233	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs145887575	chr8:125641233-125641234	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs77717998	chr8:125641247-125641248	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs11777231	chr8:125641251-125641252	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs530141268	chr8:125641258-125641259	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs549913281	chr8:125641303-125641304	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs569960496	chr8:125641305-125641306	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs538953255	chr8:125641310-125641311	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs184004060	chr8:125641386-125641387	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs188684780	chr8:125641417-125641418	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs534582641	chr8:125641462-125641463	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs77105878	chr8:125641470-125641471	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs541418938	chr8:125641482-125641483	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs574538237	chr8:125641498-125641499	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs575807731	chr8:125641526-125641527	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs557185471	chr8:125641530-125641531	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs180755435	chr8:125641556-125641557	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs183845596	chr8:125641561-125641562	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs559572714	chr8:125641571-125641572	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs62530674	chr8:125641572-125641573	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs528393575	chr8:125641581-125641582	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs540983467	chr8:125641583-125641584	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs558126232	chr8:125641587-125641588	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs560947486	chr8:125641607-125641608	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs138483702	chr8:125641674-125641675	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs549900832	chr8:125641675-125641676	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs569897942	chr8:125641679-125641680	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs71516751	chr8:125641681-125641682	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs71516752	chr8:125641693-125641694	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs142715084	chr8:125641713-125641714	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs199730322	chr8:125641735-125641736	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs59476168	chr8:125641738-125641739	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs528445558	chr8:125641741-125641742	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs554603887	chr8:125641761-125641762	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs530045667	chr8:125641763-125641764	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs370425172	chr8:125641768-125641769	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs4871522	chr8:125641773-125641774	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs118123056	chr8:125641777-125641778	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs4871523	chr8:125641779-125641780	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs537130323	chr8:125641849-125641850	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs561683976	chr8:125641882-125641883	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs576889901	chr8:125641911-125641912	Enhancers Weak transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:146)

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
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:435 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125619200-125649000	Weak transcription	Colonic Mucosa	Colon
2	chr8:125633400-125643200	Weak transcription	Fetal Kidney	kidney
3	chr8:125633800-125641000	Weak transcription	Osteobl	bone
4	chr8:125633800-125642400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr8:125634400-125641800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr8:125634800-125646600	Weak transcription	Primary T cells from cord blood	blood
7	chr8:125635800-125641000	Enhancers	Fetal Thymus	thymus
8	chr8:125635800-125641200	Enhancers	Fetal Muscle Trunk	muscle
9	chr8:125636400-125644400	Enhancers	Brain Inferior Temporal Lobe	brain
10	chr8:125636600-125641200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
11	chr8:125636600-125644000	Enhancers	Fetal Heart	heart
12	chr8:125636600-125644200	Enhancers	Placenta	Placenta
13	chr8:125636800-125641400	Enhancers	Brain Substantia Nigra	brain
14	chr8:125637000-125644200	Enhancers	Thymus	Thymus
15	chr8:125637200-125651000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
16	chr8:125637800-125644200	Enhancers	K562	blood
17	chr8:125638000-125643000	Enhancers	Brain Cingulate Gyrus	brain
18	chr8:125638000-125644200	Enhancers	Psoas Muscle	Psoas
19	chr8:125638000-125644400	Enhancers	Cortex derived primary cultured neurospheres	brain
20	chr8:125638200-125643200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr8:125638200-125644600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr8:125638600-125641800	Weak transcription	Fetal Stomach	stomach
23	chr8:125639000-125643800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr8:125639000-125643800	Enhancers	Lung	lung
25	chr8:125639200-125642200	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr8:125639200-125642400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr8:125639200-125642600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr8:125639200-125644200	Enhancers	Fetal Muscle Leg	muscle
29	chr8:125639200-125646600	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr8:125639400-125644200	Enhancers	Spleen	Spleen
31	chr8:125639600-125641200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr8:125639600-125642200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr8:125639600-125642200	Weak transcription	Stomach Mucosa	stomach
34	chr8:125639600-125649800	Weak transcription	Fetal Brain Female	brain
35	chr8:125639800-125641000	Enhancers	Primary B cells from cord blood	blood
36	chr8:125639800-125641000	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr8:125639800-125641200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
38	chr8:125639800-125641400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
39	chr8:125639800-125641600	Weak transcription	HMEC	breast
40	chr8:125639800-125641800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr8:125640000-125641000	Flanking Active TSS	GM12878-XiMat	blood
42	chr8:125640000-125641800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:125640000-125641800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:125640000-125641800	Weak transcription	Esophagus	oesophagus
45	chr8:125640000-125641800	Enhancers	Hela-S3	cervix
46	chr8:125640000-125642000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr8:125640000-125642400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr8:125640000-125642400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr8:125640000-125642400	Weak transcription	Pancreas	Pancrea
50	chr8:125640000-125646400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood

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