Variant report

Variant	esv2575696
Chromosome Location	chr6:33582877-33586760
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:43)
CpG islands
(count:61)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr6:33584824-33585044	K562	blood:	n/a	n/a
2	CEBPB	chr6:33584639-33585116	Hela-S3	cervix:	n/a	chr6:33584857-33584868
3	CEBPB	chr6:33584758-33584987	A549	lung:	n/a	chr6:33584857-33584868
4	CEBPB	chr6:33584690-33585038	IMR90	lung:	n/a	chr6:33584857-33584868
5	CEBPB	chr6:33584686-33585068	K562	blood:	n/a	chr6:33584857-33584868
6	CEBPB	chr6:33584793-33584995	HepG2	liver:	n/a	chr6:33584857-33584868
7	CEBPB	chr6:33584744-33584990	K562	blood:	n/a	chr6:33584857-33584868
8	CEBPB	chr6:33584733-33585105	K562	blood:	n/a	chr6:33584857-33584868
9	CEBPD	chr6:33584739-33585205	K562	blood:	n/a	n/a
10	CTCF	chr6:33586720-33586870	GM12872	blood:	n/a	n/a
11	EP300	chr6:33584772-33585061	K562	blood:	n/a	n/a
12	EP300	chr6:33584641-33585103	Hela-S3	cervix:	n/a	n/a
13	FOS	chr6:33584729-33585040	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr6:33584686-33585060	MCF10A-Er-Src	breast:	n/a	n/a
15	FOS	chr6:33584780-33584980	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr6:33584690-33584993	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr6:33585873-33586305	HUVEC	blood vessel:	n/a	n/a
18	GATA1	chr6:33584741-33585211	PBDE	blood:	n/a	n/a
19	GATA1	chr6:33584730-33585206	K562	blood:	n/a	n/a
20	GATA2	chr6:33584705-33585012	K562	blood:	n/a	n/a
21	GATA2	chr6:33584720-33585040	K562	blood:	n/a	n/a
22	MAX	chr6:33584677-33585047	Hela-S3	cervix:	n/a	n/a
23	MXI1	chr6:33584718-33585001	Hela-S3	cervix:	n/a	n/a
24	MYC	chr6:33584798-33584829	MCF10A-Er-Src	breast:	n/a	n/a
25	MYC	chr6:33584735-33584964	MCF10A-Er-Src	breast:	n/a	n/a
26	MYC	chr6:33586085-33586177	HUVEC	blood vessel:	n/a	n/a
27	MYC	chr6:33586595-33586627	HepG2	liver:	n/a	n/a
28	NR2F2	chr6:33584697-33585112	K562	blood:	n/a	n/a
29	POLR2A	chr6:33584488-33584536	GM12878	blood:	n/a	n/a
30	POLR2A	chr6:33584771-33585021	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr6:33584485-33584724	HepG2	liver:	n/a	n/a
32	RAD21	chr6:33584733-33585028	Hela-S3	cervix:	n/a	n/a
33	RCOR1	chr6:33584754-33585093	K562	blood:	n/a	n/a
34	RCOR1	chr6:33584737-33585028	Hela-S3	cervix:	n/a	n/a
35	RFX5	chr6:33584729-33585033	Hela-S3	cervix:	n/a	n/a
36	SMC3	chr6:33584747-33585049	Hela-S3	cervix:	n/a	n/a
37	STAT3	chr6:33584710-33585092	Hela-S3	cervix:	n/a	n/a
38	TAL1	chr6:33584737-33585063	K562	blood:	n/a	n/a
39	TBL1XR1	chr6:33584810-33585057	K562	blood:	n/a	n/a
40	TBP	chr6:33584727-33585070	Hela-S3	cervix:	n/a	n/a
41	TCF7L2	chr6:33584724-33585126	Hela-S3	cervix:	n/a	n/a
42	TEAD4	chr6:33584750-33585050	K562	blood:	n/a	n/a
43	TEAD4	chr6:33584647-33585134	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:33585071-33585121	NHDF-neo	bronchial:	n/a
2	chr6:33585071-33585121	HAEpiC	amniotic membrane:	n/a
3	chr6:33585071-33585121	HCM	heart:	n/a
4	chr6:33585071-33585121	MCF-7	breast:	n/a
5	chr6:33585071-33585121	SK-N-SH	brain:	n/a
6	chr6:33585071-33585121	H1-hESC	embryonic stem cell:	embryo
7	chr6:33585071-33585121	SK-N-MC	brain:	n/a
8	chr6:33585071-33585121	PFSK-1	brain:	n/a
9	chr6:33585071-33585121	CMK	blood:	n/a
10	chr6:33585071-33585121	HMEC	breast:	n/a
11	chr6:33585071-33585121	Hepatocyte	liver:	n/a
12	chr6:33585071-33585121	LNCaP	prostate:	n/a
13	chr6:33585071-33585121	AG04449	skin:	fetal
14	chr6:33585071-33585121	ovcar-3	ovarian:	n/a
15	chr6:33585071-33585121	GM19239	blood:	n/a
16	chr6:33585071-33585121	SK-N-SH_RA	brain:	n/a
17	chr6:33585071-33585121	AoSMC	blood vessel:	n/a
18	chr6:33585071-33585121	NH-A	brain:	n/a
19	chr6:33585071-33585121	A549	lung:	n/a
20	chr6:33585071-33585121	PrEC	prostate:	n/a
21	chr6:33585071-33585121	GM06990	blood:	n/a
22	chr6:33585071-33585121	IMR90	lung:	fetal
23	chr6:33585071-33585121	T-47D	breast:	n/a
24	chr6:33585071-33585121	HEK293	kidney:	embryo
25	chr6:33585071-33585121	NHBE	bronchial:	n/a
26	chr6:33585071-33585121	AG04450	lung:	fetal
27	chr6:33585071-33585121	GM12891	blood:	n/a
28	chr6:33585071-33585121	Caco-2	colon:	n/a
29	chr6:33585071-33585121	HCPEpiC	choroid plexus:	n/a
30	chr6:33585071-33585121	HCT-116	colon:	n/a
31	chr6:33585071-33585121	HRE	kidney:	n/a
32	chr6:33585071-33585121	HNPCEpiC	eye:	n/a
33	chr6:33585071-33585121	HUVEC	blood vessel:	n/a
34	chr6:33585071-33585121	PANC-1	pancreas:	n/a
35	chr6:33585071-33585121	AG09319	gingival:	n/a
36	chr6:33585071-33585121	U87	brain:	n/a
37	chr6:33585071-33585121	HepG2	liver:	n/a
38	chr6:33585071-33585121	HL-60	blood:	n/a
39	chr6:33585071-33585121	ProgFib	skin:	n/a
40	chr6:33585071-33585121	HRCEpiC	kidney:	n/a
41	chr6:33585071-33585121	RPTEC	kidney:	n/a
42	chr6:33585071-33585121	AG09309	skin:	n/a
43	chr6:33585071-33585121	Jurkat	blood:	n/a
44	chr6:33585071-33585121	BJ	skin:	n/a
45	chr6:33585071-33585121	SAEC	small airway:	n/a
46	chr6:33585071-33585121	NB4	blood:	n/a
47	chr6:33585071-33585121	HRPEpiC	eye:	n/a
48	chr6:33585071-33585121	AG10803	skin:	n/a
49	chr6:33585071-33585121	HCF	heart:	n/a
50	chr6:33585071-33585121	ECC-1	luminal epithelium:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:56735246..56737826-chr6:33586590..33589099,2	MCF-7	breast:
2	chr6:33557568..33558267-chr6:33586070..33586956,2	MCF-7	breast:
3	chr6:33584326..33585911-chr6:33588780..33590574,2	K562	blood:
4	chr6:33577318..33579921-chr6:33582665..33584246,2	K562	blood:
5	chr6:33576666..33582891-chr6:33586745..33591603,10	MCF-7	breast:
6	chr6:33550022..33555745-chr6:33586647..33590467,5	MCF-7	breast:
7	chr6:33581288..33583329-chr6:33600315..33602072,2	K562	blood:
8	chr6:33582787..33585683-chr6:33587089..33588741,2	K562	blood:
9	chr6:33386588..33389201-chr6:33584352..33586241,2	MCF-7	breast:

No data

Variant related genes	Relation type
ITPR3	TF binding region
ITPR3	CpG island
ENSG00000197283	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000204188	chromatin interactions
ENSG00000096433	chromatin interactions

Extended variants
information (count: 132 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:132 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112993262	chr6:33583024-33583025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs7753829	chr6:33583039-33583040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs149578542	chr6:33583086-33583087	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs7753712	chr6:33583113-33583114	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs538281703	chr6:33583116-33583117	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs553343833	chr6:33583166-33583167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs572745457	chr6:33583180-33583181	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs577940306	chr6:33583267-33583268	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs538568710	chr6:33583314-33583315	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs576576410	chr6:33583384-33583385	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544002677	chr6:33583389-33583390	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs565404213	chr6:33583421-33583422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs7754218	chr6:33583446-33583447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182411527	chr6:33583447-33583448	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs559492995	chr6:33583461-33583462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541100029	chr6:33583523-33583524	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs7754237	chr6:33583527-33583528	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs7774689	chr6:33583534-33583535	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs113162166	chr6:33583558-33583559	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs186724626	chr6:33583637-33583638	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs549550852	chr6:33583655-33583656	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs571050268	chr6:33583689-33583690	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs543477693	chr6:33583703-33583704	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570057404	chr6:33583710-33583711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs7775014	chr6:33583716-33583717	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs13203795	chr6:33583732-33583733	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs7754713	chr6:33583748-33583749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs7754720	chr6:33583764-33583765	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs35417620	chr6:33583784-33583785	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs560410431	chr6:33583789-33583790	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs570305142	chr6:33583874-33583875	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13206871	chr6:33583877-33583878	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs7758655	chr6:33583878-33583879	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs541549257	chr6:33583908-33583909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs184028336	chr6:33583928-33583929	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs113073329	chr6:33583929-33583930	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs7740889	chr6:33584003-33584004	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs187345545	chr6:33584005-33584006	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs193001428	chr6:33584021-33584022	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs147596475	chr6:33584034-33584035	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs543260845	chr6:33584099-33584100	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564739433	chr6:33584212-33584213	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs6922964	chr6:33584301-33584302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs12196962	chr6:33584332-33584333	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs185599159	chr6:33584355-33584356	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575458710	chr6:33584409-33584410	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs115443856	chr6:33584419-33584420	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs35239042	chr6:33584440-33584441	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs529682996	chr6:33584500-33584501	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs571556351	chr6:33584512-33584513	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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
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
Lung cancer	18438408	CNVD
Glioblastoma multiforme	21138945	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33574400-33583200	Enhancers	HMEC	breast
2	chr6:33577400-33583000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:33578000-33587000	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr6:33578800-33588000	Weak transcription	Gastric	stomach
5	chr6:33579000-33583800	Weak transcription	Right Ventricle	heart
6	chr6:33579200-33586600	Weak transcription	Fetal Lung	lung
7	chr6:33579200-33587000	Weak transcription	Pancreas	Pancrea
8	chr6:33579400-33587000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr6:33579400-33587000	Weak transcription	Right Atrium	heart
10	chr6:33579400-33588000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr6:33580000-33586800	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr6:33580000-33587600	Weak transcription	Brain Substantia Nigra	brain
13	chr6:33580800-33583000	Enhancers	NHDF-Ad	bronchial
14	chr6:33580800-33583400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr6:33581000-33583000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr6:33581000-33583000	Enhancers	HSMMtube	muscle
17	chr6:33581400-33583000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr6:33581600-33588000	Weak transcription	Brain Anterior Caudate	brain
19	chr6:33581800-33586800	Weak transcription	A549	lung
20	chr6:33582000-33583000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr6:33582000-33583000	Enhancers	HSMM	muscle
22	chr6:33582000-33583000	Enhancers	Osteobl	bone
23	chr6:33582000-33583200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr6:33582000-33584000	Weak transcription	Fetal Intestine Small	intestine
25	chr6:33582000-33586000	Weak transcription	Spleen	Spleen
26	chr6:33582000-33586600	Weak transcription	Placenta	Placenta
27	chr6:33582000-33586800	Weak transcription	Colonic Mucosa	Colon
28	chr6:33582000-33587000	Weak transcription	Left Ventricle	heart
29	chr6:33582000-33587400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr6:33582000-33587400	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr6:33582000-33587400	Weak transcription	NHLF	lung
32	chr6:33582200-33583200	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:33582200-33584000	Weak transcription	Fetal Intestine Large	intestine
34	chr6:33582200-33586000	Weak transcription	HUVEC	blood vessel
35	chr6:33582200-33586000	Weak transcription	NHEK	skin
36	chr6:33582200-33586800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:33582200-33587200	Enhancers	Hela-S3	cervix
38	chr6:33582200-33587800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:33582400-33586800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr6:33582400-33586800	Weak transcription	Stomach Mucosa	stomach
41	chr6:33582400-33587000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr6:33582400-33587000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr6:33582400-33587200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr6:33582400-33587200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr6:33582600-33583000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr6:33582600-33586800	Weak transcription	Lung	lung
47	chr6:33583000-33584000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr6:33583000-33584800	Weak transcription	Osteobl	bone
49	chr6:33583000-33586000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr6:33583000-33586000	Weak transcription	HSMM	muscle

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