Variant report

Variant	nsv970328
Chromosome Location	chr6:34760989-34774305
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:36)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:34773543..34776313-chr6:34779272..34782261,3	K562	blood:
2	chr6:34651137..34654420-chr6:34758676..34761167,3	MCF-7	breast:
3	chr6:34392492..34394082-chr6:34758851..34761190,2	MCF-7	breast:
4	chr6:34758724..34765323-chr6:34765815..34768873,9	MCF-7	breast:
5	chr6:34723785..34726777-chr6:34759451..34763099,4	MCF-7	breast:
6	chr6:34662945..34666396-chr6:34758284..34762755,7	K562	blood:
7	chr6:34760038..34762450-chr6:35204039..35206411,2	K562	blood:
8	chr6:34759044..34761297-chr6:34854138..34856970,2	K562	blood:
9	chr6:34773906..34776367-chr6:34780573..34782825,3	MCF-7	breast:
10	chr6:34759998..34762126-chr6:34777640..34780581,3	MCF-7	breast:
11	chr6:34766487..34768017-chr6:34768544..34771127,2	MCF-7	breast:
12	chr6:34759673..34761787-chr6:34787706..34790146,2	MCF-7	breast:
13	chr6:34761569..34764046-chr6:35162032..35164160,2	K562	blood:
14	chr6:34767361..34769871-chr6:34784104..34787037,2	K562	blood:
15	chr6:34760758..34763688-chr6:34766501..34768387,2	MCF-7	breast:
16	chr6:34765089..34766642-chr6:34780537..34783059,2	K562	blood:
17	chr6:34773594..34775363-chr6:34780371..34783229,3	K562	blood:
18	chr6:34763850..34765832-chr6:34855918..34857679,2	K562	blood:
19	chr6:34773262..34775486-chr6:34854504..34857220,2	K562	blood:
20	chr6:34758609..34760887-chr6:34760994..34763673,2	MCF-7	breast:
21	chr6:34732771..34734494-chr6:34760287..34763087,2	K562	blood:
22	chr6:34747403..34749848-chr6:34763943..34765604,2	K562	blood:
23	chr6:34759093..34761380-chr6:34773456..34776260,3	MCF-7	breast:
24	chr6:34760758..34763688-chr6:34766501..34768387,2	MCF-7	breast:
25	chr6:34769066..34771587-chr6:34778054..34780112,2	K562	blood:
26	chr6:34772137..34774417-chr6:34775291..34779142,3	K562	blood:
27	chr6:34758735..34762506-chr6:34853024..34858695,7	MCF-7	breast:
28	chr6:34723754..34729214-chr6:34758122..34762652,9	MCF-7	breast:
29	chr6:34763985..34766508-chr6:34780371..34782291,2	MCF-7	breast:
30	chr6:34663461..34666396-chr6:34758437..34761219,3	K562	blood:
31	chr6:34765054..34766624-chr6:34774758..34776417,2	K562	blood:
32	chr6:34759201..34762395-chr6:34788232..34791970,5	MCF-7	breast:
33	chr6:34765154..34767029-chr6:34793754..34796653,2	K562	blood:
34	chr6:34763567..34765463-chr6:34776356..34778910,2	MCF-7	breast:
35	chr6:34763985..34766654-chr6:34795153..34797244,4	K562	blood:
36	chr6:34766487..34768017-chr6:34768544..34771127,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000270800	chromatin interactions
ENSG00000064995	chromatin interactions
ENSG00000265123	chromatin interactions
ENSG00000124614	chromatin interactions
ENSG00000206717	chromatin interactions
ENSG00000065060	chromatin interactions
ENSG00000196821	chromatin interactions
ENSG00000124562	chromatin interactions
ENSG00000064999	chromatin interactions
ENSG00000272288	chromatin interactions
ENSG00000220643	chromatin interactions

Extended variants
information (count: 502 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:502 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560765920	chr6:34760991-34760992	Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
2	rs116545336	chr6:34761087-34761088	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
3	rs141595451	chr6:34761090-34761091	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
4	rs34480368	chr6:34761174-34761175	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs144491725	chr6:34761202-34761203	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs148416046	chr6:34761245-34761246	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs560218445	chr6:34761246-34761247	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs200735641	chr6:34761270-34761271	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs547220611	chr6:34761291-34761292	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs141616470	chr6:34761301-34761302	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs534074176	chr6:34761318-34761319	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs79344835	chr6:34761360-34761361	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs553557870	chr6:34761375-34761376	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs567503718	chr6:34761382-34761383	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
15	rs538248210	chr6:34761388-34761389	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
16	rs4713827	chr6:34761394-34761395	Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs374190371	chr6:34761423-34761424	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
18	rs556867187	chr6:34761436-34761437	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs551601802	chr6:34761440-34761441	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs568665023	chr6:34761473-34761474	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs376005564	chr6:34761477-34761478	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
22	rs62404840	chr6:34761541-34761542	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
23	rs77915750	chr6:34761561-34761562	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
24	rs572101666	chr6:34761621-34761622	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
25	rs35143960	chr6:34761675-34761676	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs9462022	chr6:34761684-34761685	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs376594730	chr6:34761699-34761700	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs200002178	chr6:34761701-34761702	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
29	rs79165849	chr6:34761702-34761703	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
30	rs71722841	chr6:34761715-34761716	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
31	rs374807059	chr6:34761731-34761732	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs531171424	chr6:34761752-34761753	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs543038131	chr6:34761783-34761784	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs185357766	chr6:34761798-34761799	Weak transcription Enhancers Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs6942040	chr6:34761809-34761810	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs71538270	chr6:34761826-34761827	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs547183614	chr6:34761828-34761829	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs545357901	chr6:34761849-34761850	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs565783792	chr6:34761857-34761858	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs6899471	chr6:34761862-34761863	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs573075318	chr6:34761918-34761919	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs527682638	chr6:34761934-34761935	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs199965299	chr6:34761935-34761936	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs567944686	chr6:34761943-34761944	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs71686659	chr6:34762005-34762006	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs372707548	chr6:34762008-34762009	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs188274018	chr6:34762051-34762052	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs371781394	chr6:34762052-34762053	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs150597377	chr6:34762054-34762055	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
50	rs193258663	chr6:34762059-34762060	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
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
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
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
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:432 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:34758200-34761000	Active TSS	iPS-15b Cell Line	embryonic stem cell
2	chr6:34758600-34761600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr6:34758800-34761000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
4	chr6:34758800-34761000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:34758800-34761000	Active TSS	HUES48 Cell Line	embryonic stem cell
6	chr6:34758800-34761000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr6:34758800-34761200	Active TSS	HUES64 Cell Line	embryonic stem cell
8	chr6:34758800-34761200	Active TSS	Pancreatic Islets	Pancreatic Islet
9	chr6:34758800-34761400	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr6:34758800-34761400	Active TSS	H9 Cell Line	embryonic stem cell
11	chr6:34758800-34761600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:34758800-34761600	Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr6:34759000-34761000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr6:34759000-34761000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr6:34759000-34761000	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr6:34759000-34761000	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
17	chr6:34759000-34761000	Active TSS	Esophagus	oesophagus
18	chr6:34759000-34761000	Active TSS	Left Ventricle	heart
19	chr6:34759000-34761000	Active TSS	Ovary	ovary
20	chr6:34759000-34761000	Active TSS	Pancreas	Pancrea
21	chr6:34759000-34761000	Active TSS	Psoas Muscle	Psoas
22	chr6:34759000-34761000	Active TSS	Right Ventricle	heart
23	chr6:34759000-34761000	Active TSS	Sigmoid Colon	Sigmoid Colon
24	chr6:34759000-34761000	Active TSS	Stomach Mucosa	stomach
25	chr6:34759000-34761000	Active TSS	NHDF-Ad	bronchial
26	chr6:34759000-34761000	Active TSS	NHLF	lung
27	chr6:34759000-34761200	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr6:34759000-34761400	Active TSS	Right Atrium	heart
29	chr6:34759000-34761400	Active TSS	HSMMtube	muscle
30	chr6:34759000-34761600	Active TSS	H1 Cell Line	embryonic stem cell
31	chr6:34759200-34761000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:34759200-34761000	Active TSS	iPS-18 Cell Line	embryonic stem cell
33	chr6:34759200-34761000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr6:34759200-34761000	Active TSS	Brain Anterior Caudate	brain
35	chr6:34759200-34761000	Active TSS	Fetal Intestine Small	intestine
36	chr6:34759200-34761000	Active TSS	Lung	lung
37	chr6:34759200-34761000	Active TSS	Rectal Smooth Muscle	rectum
38	chr6:34759200-34761000	Bivalent/Poised TSS	HepG2	liver
39	chr6:34759200-34761000	Active TSS	HSMM	muscle
40	chr6:34759200-34761200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr6:34759200-34761200	Active TSS	Colon Smooth Muscle	Colon
42	chr6:34759200-34761600	Active TSS	GM12878-XiMat	blood
43	chr6:34759400-34761000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:34759400-34761000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:34759400-34761000	Active TSS	Fetal Intestine Large	intestine
46	chr6:34759400-34761000	Active TSS	Rectal Mucosa Donor 29	rectum
47	chr6:34759400-34761000	Active TSS	Small Intestine	intestine
48	chr6:34759400-34761000	Active TSS	Hela-S3	cervix
49	chr6:34759400-34761000	Active TSS	K562	blood
50	chr6:34759400-34761000	Active TSS	Monocytes-CD14+_RO01746	blood

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