Variant report

Variant	nsv965719
Chromosome Location	chr6:35617589-35622224
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:35618904-35619528	K562	blood:	n/a	n/a
2	BHLHE40	chr6:35619105-35619412	K562	blood:	n/a	n/a
3	CEBPB	chr6:35617517-35617626	A549	lung:	n/a	chr6:35617561-35617572
4	CEBPB	chr6:35619027-35619430	K562	blood:	n/a	n/a
5	CEBPB	chr6:35619052-35619320	K562	blood:	n/a	n/a
6	CEBPB	chr6:35617494-35617635	HepG2	liver:	n/a	chr6:35617561-35617572
7	CEBPB	chr6:35619013-35619533	K562	blood:	n/a	n/a
8	CEBPD	chr6:35619038-35619512	K562	blood:	n/a	n/a
9	CEBPD	chr6:35618974-35619522	K562	blood:	n/a	n/a
10	CUX1	chr6:35619203-35619558	K562	blood:	n/a	n/a
11	EGR1	chr6:35619102-35619398	K562	blood:	n/a	n/a
12	EP300	chr6:35618931-35619431	K562	blood:	n/a	n/a
13	EP300	chr6:35618884-35619490	K562	blood:	n/a	n/a
14	GATA1	chr6:35618996-35619714	PBDE	blood:	n/a	n/a
15	GATA2	chr6:35619054-35619487	K562	blood:	n/a	n/a
16	IRF1	chr6:35619065-35619452	K562	blood:	n/a	n/a
17	IRF3	chr6:35621884-35621895	GM12878	blood:	n/a	n/a
18	JUN	chr6:35619040-35619422	K562	blood:	n/a	n/a
19	JUND	chr6:35617491-35617657	HepG2	liver:	n/a	n/a
20	JUND	chr6:35619100-35619393	K562	blood:	n/a	n/a
21	KAP1	chr6:35619231-35619431	K562	blood:	n/a	n/a
22	MAFF	chr6:35619147-35619444	K562	blood:	n/a	n/a
23	MAFK	chr6:35619228-35619447	K562	blood:	n/a	n/a
24	MAZ	chr6:35619176-35619391	K562	blood:	n/a	n/a
25	MXI1	chr6:35619089-35619224	K562	blood:	n/a	n/a
26	NR2F2	chr6:35619084-35619447	K562	blood:	n/a	n/a
27	PML	chr6:35619066-35619490	K562	blood:	n/a	n/a
28	POLR2A	chr6:35620888-35621194	GM12892	blood:	n/a	n/a
29	POLR2A	chr6:35621008-35621158	H1-hESC	embryonic stem cell:	n/a	n/a
30	POLR2A	chr6:35619549-35619816	GM12878	blood:	n/a	n/a
31	POLR2A	chr6:35620978-35621104	A549	lung:	n/a	n/a
32	POLR2A	chr6:35619589-35619740	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr6:35619106-35619335	K562	blood:	n/a	n/a
34	POLR2A	chr6:35620727-35620937	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr6:35619124-35619280	K562	blood:	n/a	n/a
36	RCOR1	chr6:35619092-35619457	K562	blood:	n/a	n/a
37	RFX5	chr6:35619529-35619597	K562	blood:	n/a	n/a
38	TAL1	chr6:35619003-35619489	K562	blood:	n/a	n/a
39	TBL1XR1	chr6:35619185-35619425	K562	blood:	n/a	n/a
40	TEAD4	chr6:35618980-35619443	K562	blood:	n/a	n/a
41	TEAD4	chr6:35618891-35619520	K562	blood:	n/a	n/a
42	UBTF	chr6:35619097-35619416	K562	blood:	n/a	n/a
43	ZMIZ1	chr6:35619098-35619433	K562	blood:	n/a	n/a
44	ZNF384	chr6:35618101-35618308	K562	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:35620486..35627650-chr6:35628500..35632953,8	K562	blood:
2	chr6:35620721..35623536-chr6:35629276..35630883,2	K562	blood:
3	chr6:35617138..35618908-chr6:35655522..35657648,2	K562	blood:
4	chr6:35615240..35617365-chr6:35622051..35624725,2	K562	blood:
5	chr6:35617868..35619553-chr6:35622560..35625369,2	K562	blood:
6	chr6:35610364..35613285-chr6:35617762..35619344,2	K562	blood:
7	chr6:35613520..35615470-chr6:35617649..35619369,2	K562	blood:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARMC12-1	chr6:35620387-35620460	NONHSAT112187
2	lnc-ARMC12-1	chr6:35620970-35621424	NONHSAT112187
3	lnc-ARMC12-1	chr6:35620623-35620688	NONHSAT112187

No data

Variant related genes	Relation type
ENSG00000212579	TF binding region
ENSG00000096060	chromatin interactions
ENSG00000265527	chromatin interactions

Extended variants
information (count: 175 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:175 , 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	rs144327633	chr6:35617602-35617603	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs115825224	chr6:35617632-35617633	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs576214323	chr6:35617633-35617634	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs188580352	chr6:35617665-35617666	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558237029	chr6:35617695-35617696	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs576940691	chr6:35617710-35617711	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs193137462	chr6:35617713-35617714	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs148017748	chr6:35617761-35617762	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs35807640	chr6:35617786-35617787	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs185661038	chr6:35617813-35617814	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4713903	chr6:35617821-35617822	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs143517763	chr6:35617887-35617888	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187784370	chr6:35617893-35617894	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs117106192	chr6:35617923-35617924	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs73417678	chr6:35617951-35617952	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547609326	chr6:35617954-35617955	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs564922291	chr6:35617979-35617980	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs63526964	chr6:35618077-35618078	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548972206	chr6:35618078-35618079	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs398001164	chr6:35618093-35618094	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs532411150	chr6:35618142-35618143	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs568230143	chr6:35618154-35618155	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147140544	chr6:35618176-35618177	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs200951563	chr6:35618180-35618181	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs565788967	chr6:35618259-35618260	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs191242235	chr6:35618262-35618263	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs140253283	chr6:35618302-35618303	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs569851437	chr6:35618326-35618327	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs536923114	chr6:35618327-35618328	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs184212997	chr6:35618399-35618400	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576905825	chr6:35618400-35618401	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs375577388	chr6:35618404-35618405	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144531793	chr6:35618472-35618473	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs376993406	chr6:35618532-35618533	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs188546110	chr6:35618542-35618543	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs536501933	chr6:35618549-35618550	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs11963207	chr6:35618594-35618595	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs541931371	chr6:35618595-35618596	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs561303705	chr6:35618610-35618611	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs77571794	chr6:35618686-35618687	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181178965	chr6:35618803-35618804	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565282620	chr6:35618829-35618830	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs532669774	chr6:35618872-35618873	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs547346410	chr6:35618877-35618878	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs570034507	chr6:35618901-35618902	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs559334569	chr6:35618902-35618903	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs530107726	chr6:35618928-35618929	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs139047884	chr6:35618929-35618930	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs541716620	chr6:35618934-35618935	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs139188176	chr6:35618974-35618975	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
Lung cancer	19153074	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD

Chromatin state (count:136 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:35588200-35630800	Weak transcription	Colonic Mucosa	Colon
2	chr6:35605000-35621600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:35608200-35622400	Weak transcription	Fetal Heart	heart
4	chr6:35609000-35622400	Weak transcription	Colon Smooth Muscle	Colon
5	chr6:35609000-35622400	Weak transcription	Esophagus	oesophagus
6	chr6:35609400-35622400	Weak transcription	Lung	lung
7	chr6:35609400-35622400	Weak transcription	Ovary	ovary
8	chr6:35609400-35630400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:35609400-35630600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr6:35609400-35630800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr6:35609400-35630800	Weak transcription	Gastric	stomach
12	chr6:35609600-35630200	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:35609600-35630600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr6:35610000-35630800	Weak transcription	Spleen	Spleen
15	chr6:35610000-35630800	Weak transcription	HMEC	breast
16	chr6:35610400-35630600	Weak transcription	Duodenum Smooth Muscle	Duodenum
17	chr6:35610600-35625000	Weak transcription	Right Ventricle	heart
18	chr6:35610600-35630000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr6:35610600-35630000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr6:35610600-35630000	Weak transcription	Pancreas	Pancrea
21	chr6:35610600-35630400	Weak transcription	HUVEC	blood vessel
22	chr6:35610600-35630800	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr6:35610600-35631200	Weak transcription	Primary hematopoietic stem cells	blood
24	chr6:35611200-35631000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr6:35611400-35630800	Weak transcription	Brain Substantia Nigra	brain
26	chr6:35611600-35630800	Weak transcription	Brain Anterior Caudate	brain
27	chr6:35611600-35631400	Weak transcription	Primary B cells from cord blood	blood
28	chr6:35612200-35630800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr6:35613400-35621800	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr6:35613400-35629800	Weak transcription	NHEK	skin
31	chr6:35613400-35630800	Weak transcription	Small Intestine	intestine
32	chr6:35613600-35630800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
33	chr6:35613600-35630800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr6:35614000-35617800	Enhancers	Primary T helper naive cells from peripheral blood	blood
35	chr6:35614000-35618000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr6:35614000-35630800	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr6:35614200-35618800	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr6:35614200-35625600	Weak transcription	Primary monocytes fromperipheralblood	blood
39	chr6:35614200-35630800	Weak transcription	Liver	Liver
40	chr6:35614400-35618600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
41	chr6:35614600-35619000	Weak transcription	Fetal Thymus	thymus
42	chr6:35614600-35619400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr6:35614600-35630800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr6:35614800-35625000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr6:35615000-35631000	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr6:35615400-35618600	Weak transcription	K562	blood
47	chr6:35615400-35635200	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr6:35615600-35618800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
49	chr6:35615600-35619200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:35615600-35620800	Weak transcription	GM12878-XiMat	blood

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