Variant report

Variant	esv988690
Chromosome Location	chr6:31879135-31884025
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:113)
CpG islands
(count:0)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:113 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31879193-31879474	K562	blood:	n/a	n/a
2	ATF3	chr6:31879212-31879447	K562	blood:	n/a	n/a
3	ATF3	chr6:31879116-31879438	K562	blood:	n/a	n/a
4	BATF	chr6:31879152-31879398	GM12878	blood:	n/a	chr6:31879356-31879367 chr6:31879331-31879342
5	BATF	chr6:31879156-31879480	GM12878	blood:	n/a	chr6:31879356-31879367 chr6:31879331-31879342
6	BCL11A	chr6:31879171-31879493	GM12878	blood:	n/a	n/a
7	CBX3	chr6:31879153-31879556	HCT-116	colon:	n/a	n/a
8	CBX3	chr6:31883065-31883640	HCT-116	colon:	n/a	n/a
9	CEBPB	chr6:31879032-31879457	IMR90	lung:	n/a	n/a
10	CEBPB	chr6:31879065-31879499	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr6:31883000-31883150	GM12873	blood:	n/a	n/a
12	CTCF	chr6:31883020-31883170	GM12871	blood:	n/a	n/a
13	CTCF	chr6:31883060-31883210	HMEC	breast:	n/a	n/a
14	CTCF	chr6:31882920-31883070	HCT-116	colon:	n/a	n/a
15	CTCF	chr6:31883000-31883150	GM12867	blood:	n/a	n/a
16	CTCF	chr6:31882980-31883130	GM12873	blood:	n/a	n/a
17	CTCF	chr6:31883240-31883390	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr6:31882960-31883110	MCF-7	breast:	n/a	n/a
19	CTCF	chr6:31883020-31883170	GM12875	blood:	n/a	n/a
20	CTCF	chr6:31883460-31883610	GM12873	blood:	n/a	n/a
21	CTCF	chr6:31883160-31883310	GM12873	blood:	n/a	n/a
22	CTCF	chr6:31883020-31883170	GM12872	blood:	n/a	n/a
23	CTCF	chr6:31883260-31883410	GM12870	blood:	n/a	n/a
24	CTCF	chr6:31883040-31883190	GM12874	blood:	n/a	n/a
25	CTCF	chr6:31883180-31883330	NHEK	skin:	n/a	n/a
26	CTCF	chr6:31882980-31883130	GM12868	blood:	n/a	n/a
27	CTCF	chr6:31883040-31883190	HepG2	liver:	n/a	n/a
28	CTCF	chr6:31883000-31883150	SAEC	small airway:	n/a	n/a
29	CTCF	chr6:31883040-31883190	SAEC	small airway:	n/a	n/a
30	CTCF	chr6:31883060-31883210	HEK293	kidney:	n/a	n/a
31	EP300	chr6:31879082-31879487	Hela-S3	cervix:	n/a	n/a
32	EP300	chr6:31879202-31879395	K562	blood:	n/a	n/a
33	ESR1	chr6:31883536-31883874	T-47D	breast:	n/a	n/a
34	FOS	chr6:31879058-31879523	MCF10A-Er-Src	breast:	n/a	chr6:31879329-31879340
35	FOS	chr6:31879041-31879552	MCF10A-Er-Src	breast:	n/a	chr6:31879329-31879340
36	FOS	chr6:31879113-31879513	HUVEC	blood vessel:	n/a	chr6:31879329-31879340
37	FOS	chr6:31880124-31880136	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:31879147-31879522	MCF10A-Er-Src	breast:	n/a	chr6:31879329-31879340
39	FOS	chr6:31879075-31879540	MCF10A-Er-Src	breast:	n/a	chr6:31879329-31879340
40	FOSL1	chr6:31879036-31879487	HCT-116	colon:	n/a	chr6:31879358-31879369 chr6:31879329-31879340
41	FOSL1	chr6:31879108-31879546	K562	blood:	n/a	chr6:31879358-31879369 chr6:31879329-31879340
42	FOSL1	chr6:31879177-31879474	K562	blood:	n/a	chr6:31879358-31879369 chr6:31879329-31879340
43	FOSL1	chr6:31879028-31879514	HCT-116	colon:	n/a	chr6:31879358-31879369 chr6:31879329-31879340
44	FOSL2	chr6:31879040-31879504	SK-N-SH	brain:	n/a	n/a
45	FOSL2	chr6:31879186-31879433	A549	lung:	n/a	n/a
46	FOSL2	chr6:31879138-31879492	HepG2	liver:	n/a	n/a
47	FOSL2	chr6:31879091-31879500	SK-N-SH	brain:	n/a	n/a
48	FOSL2	chr6:31879049-31879483	MCF-7	breast:	n/a	n/a
49	FOSL2	chr6:31879013-31879473	A549	lung:	n/a	n/a
50	FOSL2	chr6:31879107-31879462	MCF-7	breast:	n/a	n/a

No data

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31586050..31587690-chr6:31877612..31880010,2	K562	blood:
2	chr6:31869584..31871706-chr6:31883469..31885193,2	MCF-7	breast:
3	chr6:31878620..31883206-chr6:31886639..31889995,5	K562	blood:
4	chr6:31870028..31871569-chr6:31882046..31884323,2	K562	blood:
5	chr6:31881367..31885935-chr6:31919147..31922129,4	MCF-7	breast:
6	chr6:31866937..31870954-chr6:31878649..31881648,4	K562	blood:
7	chr6:31695993..31698251-chr6:31878269..31880269,2	MCF-7	breast:
8	chr6:31868484..31871109-chr6:31881429..31883570,2	K562	blood:
9	chr6:31881823..31884670-chr6:31889806..31892160,2	MCF-7	breast:
10	chr6:31865470..31869288-chr6:31882804..31884762,3	MCF-7	breast:
11	chr6:31871171..31873867-chr6:31879950..31882707,2	K562	blood:
12	chr6:31882959..31885262-chr6:31885767..31888829,3	MCF-7	breast:
13	chr6:31866937..31868698-chr6:31878649..31880716,2	K562	blood:
14	chr6:31874923..31879806-chr6:31881504..31885897,6	K562	blood:
15	chr6:31882562..31885157-chr6:31886185..31888056,2	K562	blood:
16	chr6:31878159..31881890-chr6:31886214..31889355,6	MCF-7	breast:
17	chr6:31878808..31881745-chr6:31887583..31889683,2	MCF-7	breast:
18	chr6:31874923..31879806-chr6:31881504..31885897,6	K562	blood:
19	chr6:31883893..31886674-chr6:31911662..31913312,2	MCF-7	breast:
20	chr6:31863769..31866724-chr6:31879168..31880795,3	K562	blood:

No data

Variant related genes	Relation type
C2	TF binding region
ENSG00000243649	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000204371	chromatin interactions

Extended variants
information (count: 140 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:140 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3128761	chr6:31879158-31879159	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs544668998	chr6:31879258-31879259	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs371055841	chr6:31879321-31879322	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs141202559	chr6:31879354-31879355	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs115104850	chr6:31879377-31879378	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs562801918	chr6:31879405-31879406	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs539145914	chr6:31879406-31879407	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs571719996	chr6:31879417-31879418	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs531848294	chr6:31879420-31879421	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs572418284	chr6:31879426-31879427	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs201151129	chr6:31879472-31879473	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs538628437	chr6:31879475-31879476	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs547785445	chr6:31879554-31879555	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs566227504	chr6:31879564-31879565	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs183876196	chr6:31879626-31879627	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs62395850	chr6:31879705-31879706	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs70990289	chr6:31879708-31879709	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs571590695	chr6:31879738-31879739	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs114408539	chr6:31879740-31879741	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs547360894	chr6:31879767-31879768	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs28732166	chr6:31879772-31879773	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs570221329	chr6:31879834-31879835	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs537645446	chr6:31879838-31879839	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs556265492	chr6:31879910-31879911	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs577680497	chr6:31879924-31879925	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs138882491	chr6:31880053-31880054	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs553756067	chr6:31880114-31880115	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs73404147	chr6:31880133-31880134	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs542555368	chr6:31880200-31880201	Enhancers Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs368235702	chr6:31880220-31880221	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs371996326	chr6:31880221-31880222	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs376727724	chr6:31880222-31880223	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs142000271	chr6:31880339-31880340	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs531360145	chr6:31880356-31880357	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs543238254	chr6:31880423-31880424	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs7452637	chr6:31880424-31880425	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs565200708	chr6:31880436-31880437	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs9267671	chr6:31880480-31880481	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs537234315	chr6:31880507-31880508	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs188541941	chr6:31880521-31880522	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs566113339	chr6:31880532-31880533	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs530126467	chr6:31880582-31880583	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs375090466	chr6:31880603-31880604	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs3130681	chr6:31880611-31880612	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs28664777	chr6:31880623-31880624	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs112027987	chr6:31880637-31880638	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs71768525	chr6:31880638-31880639	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs151063650	chr6:31880641-31880642	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs570383961	chr6:31880690-31880691	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs181318330	chr6:31880696-31880697	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

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
Lung cancer	18438408	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
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	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
Melanoma	17363583	CNVD
Myelofibrosis	22110671	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
Breast cancer	21364760	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
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31870800-31879200	Weak transcription	HSMM	muscle
2	chr6:31874000-31880000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr6:31874400-31879800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:31874600-31883600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:31874800-31880400	Enhancers	Hela-S3	cervix
6	chr6:31875000-31880000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr6:31875600-31882600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr6:31876200-31880200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr6:31876400-31880400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr6:31876800-31879800	Weak transcription	NH-A	brain
11	chr6:31877000-31879200	Weak transcription	A549	lung
12	chr6:31877000-31880000	Enhancers	GM12878-XiMat	blood
13	chr6:31877400-31884800	Weak transcription	Brain Anterior Caudate	brain
14	chr6:31877600-31883400	Weak transcription	HepG2	liver
15	chr6:31877800-31880000	Enhancers	Osteobl	bone
16	chr6:31878000-31880000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:31878000-31880000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr6:31878000-31880200	Enhancers	NHDF-Ad	bronchial
19	chr6:31878000-31880400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr6:31878200-31879400	Enhancers	Placenta	Placenta
21	chr6:31878200-31879400	Enhancers	NHEK	skin
22	chr6:31878400-31879600	Weak transcription	NHLF	lung
23	chr6:31878400-31879800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr6:31878800-31879400	Enhancers	HMEC	breast
25	chr6:31878800-31880000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr6:31879000-31880000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr6:31879000-31880000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr6:31879000-31880800	Enhancers	K562	blood
29	chr6:31879200-31879400	Enhancers	A549	lung
30	chr6:31879200-31880000	Enhancers	HSMM	muscle
31	chr6:31879400-31879800	Weak transcription	Placenta	Placenta
32	chr6:31879400-31881400	Weak transcription	NHEK	skin
33	chr6:31879600-31880000	Enhancers	NHLF	lung
34	chr6:31879800-31880000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr6:31879800-31880000	Enhancers	Placenta	Placenta
36	chr6:31879800-31880000	Enhancers	NH-A	brain
37	chr6:31879800-31880200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:31879800-31880200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr6:31880000-31881000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr6:31880000-31881800	Weak transcription	GM12878-XiMat	blood
41	chr6:31880000-31882800	Weak transcription	Placenta	Placenta
42	chr6:31880000-31884800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:31881000-31881200	Enhancers	Esophagus	oesophagus
44	chr6:31881000-31881400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr6:31881400-31881600	Enhancers	NHEK	skin
46	chr6:31881400-31882800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:31881400-31882800	Weak transcription	Esophagus	oesophagus
48	chr6:31881800-31882000	Enhancers	GM12878-XiMat	blood
49	chr6:31882000-31882400	Weak transcription	GM12878-XiMat	blood
50	chr6:31882400-31883200	Enhancers	GM12878-XiMat	blood

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