Variant report

Variant	esv1822053
Chromosome Location	chr6:33584788-33587443
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:116)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:116 , 50 per page) page: 1 2 3

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	chr6:33584793-33584995	HepG2	liver:	n/a	chr6:33584857-33584868
3	CEBPB	chr6:33584639-33585116	Hela-S3	cervix:	n/a	chr6:33584857-33584868
4	CEBPB	chr6:33584733-33585105	K562	blood:	n/a	chr6:33584857-33584868
5	CEBPB	chr6:33584690-33585038	IMR90	lung:	n/a	chr6:33584857-33584868
6	CEBPB	chr6:33584686-33585068	K562	blood:	n/a	chr6:33584857-33584868
7	CEBPB	chr6:33584758-33584987	A549	lung:	n/a	chr6:33584857-33584868
8	CEBPB	chr6:33584744-33584990	K562	blood:	n/a	chr6:33584857-33584868
9	CEBPD	chr6:33584739-33585205	K562	blood:	n/a	n/a
10	CTCF	chr6:33586980-33587130	GM12872	blood:	n/a	n/a
11	CTCF	chr6:33587060-33587210	WERI-Rb-1	eye:	n/a	n/a
12	CTCF	chr6:33587020-33587170	HCT-116	colon:	n/a	n/a
13	CTCF	chr6:33587140-33587290	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr6:33587020-33587170	AoAF	blood vessel:	n/a	n/a
15	CTCF	chr6:33586980-33587130	AG04449	skin:	n/a	n/a
16	CTCF	chr6:33587100-33587250	GM12865	blood:	n/a	n/a
17	CTCF	chr6:33587100-33587250	HCFaa	heart:	n/a	n/a
18	CTCF	chr6:33587280-33587430	HRE	kidney:	n/a	n/a
19	CTCF	chr6:33587040-33587190	GM12871	blood:	n/a	n/a
20	CTCF	chr6:33587180-33587450	NHEK	skin:	n/a	n/a
21	CTCF	chr6:33587080-33587230	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr6:33587240-33587390	RPTEC	kidney:	n/a	n/a
23	CTCF	chr6:33587080-33587230	NHDF-neo	bronchial:	n/a	n/a
24	CTCF	chr6:33587040-33587190	HMEC	breast:	n/a	n/a
25	CTCF	chr6:33587020-33587170	GM12875	blood:	n/a	n/a
26	CTCF	chr6:33587020-33587170	A549	lung:	n/a	n/a
27	CTCF	chr6:33587020-33587170	AG04449	skin:	n/a	n/a
28	CTCF	chr6:33587035-33587207	MCF-7	breast:	n/a	n/a
29	CTCF	chr6:33587100-33587250	GM12873	blood:	n/a	n/a
30	CTCF	chr6:33587074-33587183	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:33587080-33587230	HFF	foreskin:	n/a	n/a
32	CTCF	chr6:33587060-33587210	SAEC	small airway:	n/a	n/a
33	CTCF	chr6:33587060-33587210	HPF	lung:	n/a	n/a
34	CTCF	chr6:33587080-33587230	HRPEpiC	eye:	n/a	n/a
35	CTCF	chr6:33587060-33587210	GM12872	blood:	n/a	n/a
36	CTCF	chr6:33586920-33587070	HRE	kidney:	n/a	n/a
37	CTCF	chr6:33587080-33587230	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr6:33587100-33587250	HCT-116	colon:	n/a	n/a
39	CTCF	chr6:33587260-33587410	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr6:33587100-33587250	HEK293	kidney:	n/a	n/a
41	CTCF	chr6:33587000-33587150	GM12869	blood:	n/a	n/a
42	CTCF	chr6:33587360-33587510	SAEC	small airway:	n/a	n/a
43	CTCF	chr6:33587065-33587141	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr6:33587020-33587170	AG10803	skin:	n/a	n/a
45	CTCF	chr6:33587060-33587210	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:33587080-33587230	GM12873	blood:	n/a	n/a
47	CTCF	chr6:33587080-33587230	NHEK	skin:	n/a	n/a
48	CTCF	chr6:33587080-33587230	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr6:33587100-33587250	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr6:33587049-33587190	MCF-7	breast:	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	SKMC	muscle:	n/a
2	chr6:33585071-33585121	HCPEpiC	choroid plexus:	n/a
3	chr6:33585071-33585121	HMEC	breast:	n/a
4	chr6:33585071-33585121	GM12892	blood:	n/a
5	chr6:33585071-33585121	HRE	kidney:	n/a
6	chr6:33585071-33585121	Caco-2	colon:	n/a
7	chr6:33585071-33585121	HRPEpiC	eye:	n/a
8	chr6:33585071-33585121	HEEpiC	esophagus:	n/a
9	chr6:33585071-33585121	Hepatocyte	liver:	n/a
10	chr6:33585071-33585121	K562	blood:	n/a
11	chr6:33585071-33585121	HCT-116	colon:	n/a
12	chr6:33585071-33585121	AG09309	skin:	n/a
13	chr6:33585071-33585121	HAEpiC	amniotic membrane:	n/a
14	chr6:33585071-33585121	T-47D	breast:	n/a
15	chr6:33585071-33585121	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:33585071-33585121	Hela-S3	cervix:	n/a
17	chr6:33585071-33585121	ECC-1	luminal epithelium:	n/a
18	chr6:33585071-33585121	AG04449	skin:	fetal
19	chr6:33585071-33585121	GM12891	blood:	n/a
20	chr6:33585071-33585121	HCF	heart:	n/a
21	chr6:33585071-33585121	NHDF-neo	bronchial:	n/a
22	chr6:33585071-33585121	PFSK-1	brain:	n/a
23	chr6:33585071-33585121	GM06990	blood:	n/a
24	chr6:33585071-33585121	U87	brain:	n/a
25	chr6:33585071-33585121	SAEC	small airway:	n/a
26	chr6:33585071-33585121	GM19239	blood:	n/a
27	chr6:33585071-33585121	SK-N-SH_RA	brain:	n/a
28	chr6:33585071-33585121	PrEC	prostate:	n/a
29	chr6:33585071-33585121	HEK293	kidney:	embryo
30	chr6:33585071-33585121	AG04450	lung:	fetal
31	chr6:33585071-33585121	AoSMC	blood vessel:	n/a
32	chr6:33585071-33585121	AG10803	skin:	n/a
33	chr6:33585071-33585121	MCF-7	breast:	n/a
34	chr6:33585071-33585121	SK-N-SH	brain:	n/a
35	chr6:33585071-33585121	NB4	blood:	n/a
36	chr6:33585071-33585121	HIPEpiC	eye:	n/a
37	chr6:33585071-33585121	HepG2	liver:	n/a
38	chr6:33585071-33585121	HUVEC	blood vessel:	n/a
39	chr6:33585071-33585121	H1-hESC	embryonic stem cell:	embryo
40	chr6:33585071-33585121	BJ	skin:	n/a
41	chr6:33585071-33585121	LNCaP	prostate:	n/a
42	chr6:33585071-33585121	PANC-1	pancreas:	n/a
43	chr6:33585071-33585121	BE2_C	brain:	n/a
44	chr6:33585071-33585121	IMR90	lung:	fetal
45	chr6:33585071-33585121	NHBE	bronchial:	n/a
46	chr6:33585071-33585121	CMK	blood:	n/a
47	chr6:33585071-33585121	NH-A	brain:	n/a
48	chr6:33585071-33585121	AG09319	gingival:	n/a
49	chr6:33585071-33585121	Jurkat	blood:	n/a
50	chr6:33585071-33585121	ovcar-3	ovarian:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:33582787..33585683-chr6:33587089..33588741,2	K562	blood:
2	chr6:33386588..33389201-chr6:33584352..33586241,2	MCF-7	breast:
3	chr6:33557568..33558267-chr6:33586070..33586956,2	MCF-7	breast:
4	chr6:33584326..33585911-chr6:33588780..33590574,2	K562	blood:
5	chr6:33587172..33590152-chr6:34203876..34205466,2	K562	blood:
6	chr6:33550022..33555745-chr6:33586647..33590467,5	MCF-7	breast:
7	chr17:56735246..56737826-chr6:33586590..33589099,2	MCF-7	breast:

No data

Variant related genes	Relation type
ITPR3	TF binding region
ITPR3	CpG island
ENSG00000137309	chromatin interactions
ENSG00000096433	chromatin interactions
ENSG00000204188	chromatin interactions
ENSG00000197283	chromatin interactions
ENSG00000202077	chromatin interactions

Extended variants
information (count: 91 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:91 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6924368	chr6:33584830-33584831	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs76496563	chr6:33584846-33584847	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs148891242	chr6:33585019-33585020	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs564802495	chr6:33585071-33585072	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs113891262	chr6:33585149-33585150	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs150136818	chr6:33585177-33585178	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs576153370	chr6:33585181-33585182	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs6928896	chr6:33585218-33585219	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs13197265	chr6:33585251-33585252	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs576809260	chr6:33585329-33585330	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs181226458	chr6:33585334-33585335	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547922558	chr6:33585340-33585341	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs563274651	chr6:33585344-33585345	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs74565137	chr6:33585348-33585349	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs76448144	chr6:33585349-33585350	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs70996789	chr6:33585350-33585351	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs79484727	chr6:33585351-33585352	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs78826438	chr6:33585352-33585353	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs530485962	chr6:33585414-33585415	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs552927937	chr6:33585421-33585422	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs148032330	chr6:33585440-33585441	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs535269564	chr6:33585465-33585466	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs70996790	chr6:33585513-33585514	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs386406643	chr6:33585514-33585515	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs386406644	chr6:33585525-33585526	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs560447371	chr6:33585541-33585542	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs77105782	chr6:33585558-33585559	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs547162535	chr6:33585578-33585579	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs568508025	chr6:33585617-33585618	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs535948611	chr6:33585633-33585634	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs12212749	chr6:33585693-33585694	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs185881496	chr6:33585770-33585771	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs527954493	chr6:33585799-33585800	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs562320023	chr6:33585824-33585825	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs575251243	chr6:33585839-33585840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs55908295	chr6:33585840-33585841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs141757647	chr6:33585904-33585905	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs190153922	chr6:33585938-33585939	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs181851862	chr6:33585989-33585990	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs9348920	chr6:33586057-33586058	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs540905450	chr6:33586150-33586151	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs9348921	chr6:33586179-33586180	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs377407903	chr6:33586248-33586249	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs528122126	chr6:33586252-33586253	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs541927066	chr6:33586256-33586257	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs563345919	chr6:33586261-33586262	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs530552405	chr6:33586262-33586263	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs9461893	chr6:33586264-33586265	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs187020497	chr6:33586304-33586305	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs528779235	chr6:33586327-33586328	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

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
Schizophrenia	23813976	CNVD

Chromatin state (count:176 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33578000-33587000	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr6:33578800-33588000	Weak transcription	Gastric	stomach
3	chr6:33579200-33586600	Weak transcription	Fetal Lung	lung
4	chr6:33579200-33587000	Weak transcription	Pancreas	Pancrea
5	chr6:33579400-33587000	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr6:33579400-33587000	Weak transcription	Right Atrium	heart
7	chr6:33579400-33588000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr6:33580000-33586800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr6:33580000-33587600	Weak transcription	Brain Substantia Nigra	brain
10	chr6:33581600-33588000	Weak transcription	Brain Anterior Caudate	brain
11	chr6:33581800-33586800	Weak transcription	A549	lung
12	chr6:33582000-33586000	Weak transcription	Spleen	Spleen
13	chr6:33582000-33586600	Weak transcription	Placenta	Placenta
14	chr6:33582000-33586800	Weak transcription	Colonic Mucosa	Colon
15	chr6:33582000-33587000	Weak transcription	Left Ventricle	heart
16	chr6:33582000-33587400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr6:33582000-33587400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr6:33582000-33587400	Weak transcription	NHLF	lung
19	chr6:33582200-33586000	Weak transcription	HUVEC	blood vessel
20	chr6:33582200-33586000	Weak transcription	NHEK	skin
21	chr6:33582200-33586800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr6:33582200-33587200	Enhancers	Hela-S3	cervix
23	chr6:33582200-33587800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr6:33582400-33586800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr6:33582400-33586800	Weak transcription	Stomach Mucosa	stomach
26	chr6:33582400-33587000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr6:33582400-33587000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr6:33582400-33587200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:33582400-33587200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:33582600-33586800	Weak transcription	Lung	lung
31	chr6:33583000-33584800	Weak transcription	Osteobl	bone
32	chr6:33583000-33586000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr6:33583000-33586000	Weak transcription	HSMM	muscle
34	chr6:33583000-33586600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr6:33583000-33586600	Weak transcription	NHDF-Ad	bronchial
36	chr6:33583000-33587000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr6:33583000-33587000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:33583000-33587000	Weak transcription	HSMMtube	muscle
39	chr6:33583200-33586000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr6:33583200-33586600	Weak transcription	HMEC	breast
41	chr6:33583200-33587000	Weak transcription	Muscle Satellite Cultured Cells	--
42	chr6:33583800-33585000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr6:33583800-33587800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
44	chr6:33584000-33585400	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr6:33584000-33585400	Enhancers	Fetal Intestine Large	intestine
46	chr6:33584000-33587800	Enhancers	Fetal Intestine Small	intestine
47	chr6:33584200-33586000	Enhancers	Primary T cells fromperipheralblood	blood
48	chr6:33584200-33586200	Enhancers	Primary T cells from cord blood	blood
49	chr6:33584200-33586600	Weak transcription	Right Ventricle	heart
50	chr6:33584400-33585200	Enhancers	Primary T helper naive cells fromperipheralblood	blood

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