Variant report

Variant	nsv1032074
Chromosome Location	chr6:33795671-33835988
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:76)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:76 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:33819522..33821091-chr6:33827275..33829014,2	K562	blood:
2	chr6:33827215..33829847-chr6:33845943..33848537,2	MCF-7	breast:
3	chr6:33785785..33787790-chr6:33794712..33797065,2	K562	blood:
4	chr6:33816600..33819400-chr6:33825889..33827498,2	MCF-7	breast:
5	chr6:33830042..33832096-chr6:33833170..33835454,2	MCF-7	breast:
6	chr6:33806579..33810585-chr6:33811997..33816952,7	K562	blood:
7	chr6:33725421..33728114-chr6:33818801..33821160,2	MCF-7	breast:
8	chr6:33832364..33832867-chr6:33864511..33865252,2	MCF-7	breast:
9	chr6:33828653..33831388-chr6:33831678..33834637,3	K562	blood:
10	chr6:33795530..33798300-chr6:33803409..33806426,4	MCF-7	breast:
11	chr6:33795996..33798344-chr6:33806425..33808689,2	K562	blood:
12	chr6:33797997..33800270-chr6:33808477..33810957,2	K562	blood:
13	chr6:33819522..33821091-chr6:33827275..33829014,2	K562	blood:
14	chr6:33830042..33832096-chr6:33833170..33835454,2	MCF-7	breast:
15	chr6:33798654..33800240-chr6:33803211..33805039,2	K562	blood:
16	chr6:33819352..33820057-chr6:33935715..33936362,3	MCF-7	breast:
17	chr6:33822070..33824859-chr6:33826063..33828962,3	K562	blood:
18	chr6:33791904..33795612-chr6:33806607..33809462,3	K562	blood:
19	chr6:33829206..33831689-chr6:33838290..33840301,2	MCF-7	breast:
20	chr6:33798654..33800240-chr6:33803211..33805039,2	K562	blood:
21	chr6:33780937..33783076-chr6:33806668..33808410,2	K562	blood:
22	chr6:33793637..33795279-chr6:33797318..33799112,2	MCF-7	breast:
23	chr6:33796210..33797861-chr6:33802037..33804475,2	MCF-7	breast:
24	chr6:33815385..33820274-chr6:33821193..33824652,6	K562	blood:
25	chr6:33812945..33816387-chr6:33817009..33820536,6	K562	blood:
26	chr6:33794613..33797241-chr6:33797718..33800343,2	K562	blood:
27	chr6:33819810..33820341-chr6:33995193..33995933,2	MCF-7	breast:
28	chr6:33829053..33831890-chr6:33860061..33862038,2	K562	blood:
29	chr6:33817908..33819651-chr6:33841699..33844264,2	K562	blood:
30	chr6:33802445..33804788-chr6:33817259..33819823,2	K562	blood:
31	chr6:33784583..33786250-chr6:33808935..33810623,2	MCF-7	breast:
32	chr6:33799065..33803974-chr6:33805952..33809817,6	MCF-7	breast:
33	chr6:33764445..33767119-chr6:33821769..33823685,2	MCF-7	breast:
34	chr6:33819423..33820326-chr6:33995229..33996032,2	K562	blood:
35	chr6:33828985..33830562-chr6:33833456..33836165,2	MCF-7	breast:
36	chr6:28701062..28703950-chr6:33822430..33824102,2	MCF-7	breast:
37	chr6:33784923..33786692-chr6:33819953..33822581,2	K562	blood:
38	chr6:33828985..33830562-chr6:33833456..33836165,2	MCF-7	breast:
39	chr6:33811878..33813846-chr6:33820796..33822819,2	K562	blood:
40	chr6:33795530..33798300-chr6:33803409..33806426,4	MCF-7	breast:
41	chr6:33819439..33820478-chr6:33995355..33996344,6	MCF-7	breast:
42	chr6:33819160..33821493-chr6:33955535..33958926,3	MCF-7	breast:
43	chr6:33819382..33820118-chr6:34034290..34034944,2	MCF-7	breast:
44	chr6:33822070..33824859-chr6:33826063..33828962,3	K562	blood:
45	chr6:33748572..33751307-chr6:33828989..33830767,2	K562	blood:
46	chr6:33803493..33805484-chr6:33850755..33853527,2	K562	blood:
47	chr6:33802445..33804788-chr6:33817259..33819823,2	K562	blood:
48	chr6:33788574..33790183-chr6:33793587..33795973,2	MCF-7	breast:
49	chr6:33819661..33820304-chr6:33935521..33936307,2	MCF-7	breast:
50	chr6:33795996..33798344-chr6:33806425..33808689,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ITPR3-3	chr6:33835544-33835623	NONHSAT109010
2	lnc-ITPR3-3	chr6:33824053-33824215	NONHSAT109010
3	lnc-MLN-1	chr6:33835283-33835603	ENSG00000249346
4	lnc-ITPR3-3	chr6:33824053-33824215	NONHSAT109011

No data

Variant related genes	Relation type
ENSG00000271362	chromatin interactions
ENSG00000249346	chromatin interactions
ENSG00000233183	chromatin interactions
ENSG00000161904	chromatin interactions
CHORDC1	miRNA target sites

Extended variants
information (count: 1778 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:1778 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9469602	chr6:33795671-33795672	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188702540	chr6:33795728-33795729	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs373595982	chr6:33795816-33795817	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs531629285	chr6:33795819-33795820	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs577566203	chr6:33795845-33795846	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs550146513	chr6:33795930-33795931	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs10947450	chr6:33795964-33795965	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs144972160	chr6:33796000-33796001	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs72657681	chr6:33796009-33796010	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs566979026	chr6:33796102-33796103	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs191955358	chr6:33796108-33796109	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs73747329	chr6:33796109-33796110	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs151297525	chr6:33796130-33796131	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs73747330	chr6:33796133-33796134	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs531669254	chr6:33796164-33796165	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs73747331	chr6:33796168-33796169	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs185363626	chr6:33796174-33796175	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs140528986	chr6:33796200-33796201	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs9461913	chr6:33796260-33796261	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs9461914	chr6:33796266-33796267	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs561133799	chr6:33796307-33796308	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs548205349	chr6:33796314-33796315	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs531538096	chr6:33796343-33796344	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs113812520	chr6:33796362-33796363	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs73747332	chr6:33796411-33796412	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs9461915	chr6:33796481-33796482	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs551731892	chr6:33796496-33796497	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs566790238	chr6:33796526-33796527	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs550421117	chr6:33796578-33796579	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs79850527	chr6:33796592-33796593	Enhancers Bivalent Enhancer Genic enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs145496313	chr6:33796601-33796602	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567471525	chr6:33796611-33796612	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs571750456	chr6:33796627-33796628	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs538056068	chr6:33796669-33796670	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs370359261	chr6:33796671-33796672	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538806172	chr6:33796685-33796686	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556404330	chr6:33796723-33796724	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs571628644	chr6:33796738-33796739	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs56139489	chr6:33796793-33796794	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs9461916	chr6:33796794-33796795	Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs367991031	chr6:33796819-33796820	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs571993497	chr6:33796881-33796882	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs536299849	chr6:33796918-33796919	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372212369	chr6:33796929-33796930	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs73747334	chr6:33796943-33796944	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs554648955	chr6:33796952-33796953	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs73747335	chr6:33796962-33796963	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs565107490	chr6:33797002-33797003	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs9461917	chr6:33797009-33797010	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs77210008	chr6:33797019-33797020	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:107)

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
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
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:832 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33790800-33796000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr6:33790800-33796000	Weak transcription	Right Ventricle	heart
3	chr6:33791000-33796000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr6:33791000-33796200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr6:33791000-33796400	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr6:33791600-33796400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:33792600-33795800	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr6:33792800-33795800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:33792800-33797000	Weak transcription	Ovary	ovary
10	chr6:33793000-33795800	Weak transcription	Fetal Kidney	kidney
11	chr6:33793000-33795800	Weak transcription	Rectal Smooth Muscle	rectum
12	chr6:33793000-33795800	Weak transcription	A549	lung
13	chr6:33793000-33796000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr6:33793000-33798800	Weak transcription	Spleen	Spleen
15	chr6:33794200-33795800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:33794400-33796000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr6:33794600-33796600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr6:33794600-33796600	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr6:33794600-33799400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr6:33794800-33795800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr6:33794800-33796400	Enhancers	Stomach Smooth Muscle	stomach
22	chr6:33795000-33796000	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr6:33795000-33796000	Enhancers	Osteobl	bone
24	chr6:33795000-33796200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr6:33795000-33796200	Enhancers	Duodenum Mucosa	Duodenum
26	chr6:33795000-33796200	Enhancers	Fetal Intestine Large	intestine
27	chr6:33795000-33796200	Enhancers	HSMMtube	muscle
28	chr6:33795000-33796600	Enhancers	Fetal Intestine Small	intestine
29	chr6:33795000-33799600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr6:33795200-33795800	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr6:33795200-33796000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr6:33795200-33796000	Enhancers	Brain Cingulate Gyrus	brain
33	chr6:33795200-33796000	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr6:33795200-33796200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:33795200-33796400	Bivalent Enhancer	HepG2	liver
36	chr6:33795400-33796000	Enhancers	Colonic Mucosa	Colon
37	chr6:33795400-33797200	Enhancers	H1 Cell Line	embryonic stem cell
38	chr6:33795600-33796000	Bivalent Enhancer	NH-A	brain
39	chr6:33795600-33797000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:33795600-33797200	Enhancers	Colon Smooth Muscle	Colon
41	chr6:33795800-33796200	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr6:33795800-33796400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
43	chr6:33795800-33796400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr6:33795800-33796400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr6:33795800-33796600	Enhancers	Rectal Smooth Muscle	rectum
46	chr6:33795800-33796600	Enhancers	A549	lung
47	chr6:33795800-33797000	Enhancers	Fetal Kidney	kidney
48	chr6:33795800-33797200	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
49	chr6:33795800-33797200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
50	chr6:33795800-33798000	Enhancers	HUES48 Cell Line	embryonic stem cell

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