Variant report

Variant	nsv969387
Chromosome Location	chr6:33365795-33371279
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:63)
CpG islands
(count:0)
Chromatin interactive
region (count:14)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:63 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr6:33368092-33368378	GM12878	blood:	n/a	n/a
2	FOSL2	chr6:33368056-33368327	HepG2	liver:	n/a	n/a
3	HEY1	chr6:33368249-33368448	HepG2	liver:	n/a	n/a
4	HEY1	chr6:33368293-33368470	HepG2	liver:	n/a	n/a
5	HEY1	chr6:33368223-33368452	K562	blood:	n/a	n/a
6	HEY1	chr6:33368163-33368534	K562	blood:	n/a	n/a
7	PAX5	chr6:33368016-33368382	GM12878	blood:	n/a	n/a
8	POLR2A	chr6:33369741-33369759	K562	blood:	n/a	n/a
9	POLR2A	chr6:33368084-33368474	Hela-S3	cervix:	n/a	n/a
10	POLR2A	chr6:33371268-33371814	GM12892	blood:	n/a	n/a
11	POLR2A	chr6:33369973-33370039	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr6:33370349-33370791	HepG2	liver:	n/a	n/a
13	POLR2A	chr6:33368018-33368481	GM12891	blood:	n/a	n/a
14	POLR2A	chr6:33371222-33371236	HUVEC	blood vessel:	n/a	n/a
15	POLR2A	chr6:33370644-33376342	K562	blood:	n/a	n/a
16	POLR2A	chr6:33370824-33371159	GM12878	blood:	n/a	n/a
17	POLR2A	chr6:33367819-33368563	GM12892	blood:	n/a	n/a
18	POLR2A	chr6:33370482-33370544	K562	blood:	n/a	n/a
19	POLR2A	chr6:33367269-33367623	K562	blood:	n/a	n/a
20	POLR2A	chr6:33371042-33371113	HepG2	liver:	n/a	n/a
21	POLR2A	chr6:33365292-33365815	K562	blood:	n/a	n/a
22	POLR2A	chr6:33369197-33369519	K562	blood:	n/a	n/a
23	POLR2A	chr6:33370411-33372238	K562	blood:	n/a	n/a
24	POLR2A	chr6:33365786-33366179	K562	blood:	n/a	n/a
25	POLR2A	chr6:33367776-33368500	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr6:33367854-33368454	GM12878	blood:	n/a	n/a
27	POLR2A	chr6:33365701-33366023	K562	blood:	n/a	n/a
28	POLR2A	chr6:33368083-33368440	GM12891	blood:	n/a	n/a
29	POLR2A	chr6:33371041-33371681	K562	blood:	n/a	n/a
30	POLR2A	chr6:33366667-33366696	K562	blood:	n/a	n/a
31	POLR2A	chr6:33368180-33368434	K562	blood:	n/a	n/a
32	POLR2A	chr6:33367777-33368554	GM12892	blood:	n/a	n/a
33	POLR2A	chr6:33367834-33368585	GM12878	blood:	n/a	n/a
34	POLR2A	chr6:33367967-33368519	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr6:33368148-33368451	GM12878	blood:	n/a	n/a
36	POLR2A	chr6:33369854-33369868	HepG2	liver:	n/a	n/a
37	POLR2A	chr6:33370771-33371771	SK-N-MC	brain:	n/a	n/a
38	POLR2A	chr6:33370977-33371879	PFSK-1	brain:	n/a	n/a
39	POLR2A	chr6:33370866-33370876	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr6:33368070-33368436	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr6:33369906-33370114	K562	blood:	n/a	n/a
42	POLR2A	chr6:33368023-33368217	K562	blood:	n/a	n/a
43	POLR2A	chr6:33366968-33367143	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr6:33370975-33371785	K562	blood:	n/a	n/a
45	POLR2A	chr6:33371028-33371399	Hela-S3	cervix:	n/a	n/a
46	POLR2A	chr6:33368233-33368447	A549	lung:	n/a	n/a
47	POLR2A	chr6:33370994-33370999	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr6:33369044-33369327	K562	blood:	n/a	n/a
49	POLR2A	chr6:33369984-33370060	HepG2	liver:	n/a	n/a
50	POLR2A	chr6:33371107-33371132	HUVEC	blood vessel:	n/a	n/a

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:33255817..33257369-chr6:33364679..33367095,2	K562	blood:
2	chr6:33356271..33363521-chr6:33371085..33380351,32	K562	blood:
3	chr6:33363619..33367715-chr6:33369432..33373076,4	K562	blood:
4	chr6:33366608..33368247-chr6:33376462..33378479,2	MCF-7	breast:
5	chr6:33365854..33369434-chr6:33385468..33388336,3	K562	blood:
6	chr6:33366134..33368081-chr6:33369607..33371884,2	MCF-7	breast:
7	chr6:33245690..33247274-chr6:33369658..33371309,2	MCF-7	breast:
8	chr6:33237328..33248026-chr6:33370896..33379989,29	K562	blood:
9	chr6:33368532..33370764-chr6:33391909..33394175,2	K562	blood:
10	chr6:33341840..33344393-chr6:33370227..33373059,2	K562	blood:
11	chr6:33362550..33366699-chr6:33373091..33374833,4	MCF-7	breast:
12	chr6:33237079..33247876-chr6:33369927..33381738,26	K562	blood:
13	chr6:33363619..33367715-chr6:33369432..33373076,4	K562	blood:
14	chr6:33289755..33292070-chr6:33364060..33366187,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PHF1-1	chr6:33367540-33368371	NONHSAT108992

No data

Variant related genes	Relation type
RPL12P1	TF binding region
KIFC1	TF binding region
ENSG00000227057	chromatin interactions
ENSG00000204220	chromatin interactions
ENSG00000112514	chromatin interactions
ENSG00000197283	chromatin interactions
ENSG00000112511	chromatin interactions
ENSG00000204209	chromatin interactions
ENSG00000223501	chromatin interactions
ENSG00000235863	chromatin interactions
ENSG00000237649	chromatin interactions
ENSG00000225644	chromatin interactions
ENSG00000231500	chromatin interactions

Extended variants
information (count: 194 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:194 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373212856	chr6:33365800-33365801	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs142060160	chr6:33365808-33365809	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs148906071	chr6:33365813-33365814	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs143580319	chr6:33365817-33365818	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs371607857	chr6:33365820-33365821	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs200034537	chr6:33365842-33365843	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs148040365	chr6:33365873-33365874	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs141718768	chr6:33365875-33365876	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs145995335	chr6:33365907-33365908	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs368144446	chr6:33365934-33365935	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs371690472	chr6:33365953-33365954	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs188458727	chr6:33365965-33365966	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs201747101	chr6:33365977-33365978	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs181303555	chr6:33365978-33365979	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs151153920	chr6:33365982-33365983	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs374434798	chr6:33365986-33365987	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs536932436	chr6:33366028-33366029	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs201829505	chr6:33366068-33366069	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs73741830	chr6:33366087-33366088	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs201985698	chr6:33366183-33366184	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs376756232	chr6:33366251-33366252	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs371505600	chr6:33366252-33366253	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs537547705	chr6:33366269-33366270	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs62407901	chr6:33366272-33366273	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs577184662	chr6:33366365-33366366	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs541039901	chr6:33366366-33366367	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs553310583	chr6:33366395-33366396	Weak transcription Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs572285000	chr6:33366482-33366483	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs542503924	chr6:33366488-33366489	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs373024138	chr6:33366533-33366534	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs565866417	chr6:33366553-33366554	Weak transcription Strong transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs145281137	chr6:33366609-33366610	Strong transcription Weak transcription	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs538184786	chr6:33366685-33366686	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs76507538	chr6:33366689-33366690	Strong transcription Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs373122849	chr6:33366719-33366720	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs147645361	chr6:33366753-33366754	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs564791062	chr6:33366808-33366809	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs376121402	chr6:33366830-33366831	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs184943147	chr6:33366861-33366862	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs532152748	chr6:33366863-33366864	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs370751572	chr6:33366864-33366865	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs189869238	chr6:33366871-33366872	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs374472446	chr6:33366939-33366940	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs142126889	chr6:33366955-33366956	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs530466587	chr6:33366959-33366960	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs577582798	chr6:33366964-33366965	Strong transcription Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs548854576	chr6:33366979-33366980	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs145962575	chr6:33367025-33367026	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs181927529	chr6:33367026-33367027	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs570884731	chr6:33367050-33367051	Strong transcription Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:111)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Autoimmune disease	19135723	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Myelofibrosis	22110671	CNVD
Incontinentia Pigmenti	22033527	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Encephalopathy	20692195	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Immune disease	17576883	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33360000-33371000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr6:33360000-33377400	Weak transcription	Small Intestine	intestine
3	chr6:33360000-33377600	Weak transcription	Right Atrium	heart
4	chr6:33360400-33377600	Weak transcription	Esophagus	oesophagus
5	chr6:33360400-33377600	Weak transcription	Lung	lung
6	chr6:33360800-33365800	Weak transcription	Stomach Mucosa	stomach
7	chr6:33360800-33371000	Weak transcription	Placenta	Placenta
8	chr6:33360800-33371200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr6:33360800-33377200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr6:33361000-33371000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr6:33361000-33371200	Weak transcription	Gastric	stomach
12	chr6:33361000-33371400	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr6:33361000-33372600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr6:33361000-33377200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr6:33361200-33365800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr6:33361200-33366000	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr6:33361200-33366600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr6:33361200-33370600	Weak transcription	Fetal Intestine Large	intestine
19	chr6:33361200-33371000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr6:33361200-33371200	Weak transcription	Spleen	Spleen
21	chr6:33361200-33371400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr6:33361200-33377200	Weak transcription	Colonic Mucosa	Colon
23	chr6:33361200-33377800	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr6:33361400-33371200	Weak transcription	Fetal Kidney	kidney
25	chr6:33361600-33369800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr6:33361600-33377200	Weak transcription	Primary B cells from cord blood	blood
27	chr6:33362200-33377600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr6:33362400-33365800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr6:33362400-33371200	Weak transcription	Fetal Brain Female	brain
30	chr6:33362800-33376200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr6:33363000-33376400	Strong transcription	HUES64 Cell Line	embryonic stem cell
32	chr6:33363000-33376400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
33	chr6:33363200-33369200	Weak transcription	Fetal Lung	lung
34	chr6:33363200-33370600	Weak transcription	A549	lung
35	chr6:33363200-33371400	Weak transcription	Brain Germinal Matrix	brain
36	chr6:33363200-33377200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:33363200-33377200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:33363400-33365800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr6:33363400-33365800	Weak transcription	NHEK	skin
40	chr6:33363400-33366000	Genic enhancers	Dnd41	blood
41	chr6:33363400-33367200	Weak transcription	NHDF-Ad	bronchial
42	chr6:33363400-33371000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:33363400-33376400	Strong transcription	Fetal Thymus	thymus
44	chr6:33363400-33377200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr6:33363400-33377200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:33363600-33365800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:33363600-33366600	Weak transcription	NH-A	brain
48	chr6:33364000-33366800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr6:33364000-33368400	Weak transcription	NHLF	lung
50	chr6:33364000-33377200	Weak transcription	Fetal Heart	heart

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