Variant report

Variant	esv3327396
Chromosome Location	chr15:41232885-41235433
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:37)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:37 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:41234112..41234673-chr15:41314434..41315104,2	MCF-7	breast:
2	chr15:41233308..41234007-chrX:48958051..48958896,2	Hela-S3	cervix:
3	chr15:41231932..41234904-chr15:41266157..41268211,2	K562	blood:
4	chr11:62608653..62609556-chr15:41233703..41234613,3	HCT-116	colon:
5	chr15:41232897..41235509-chr15:41313138..41315009,3	MCF-7	breast:
6	chr15:41195653..41200412-chr15:41230792..41235632,4	MCF-7	breast:
7	chr15:41206994..41209856-chr15:41231483..41234125,2	MCF-7	breast:
8	chr15:41232446..41235218-chr15:41255104..41257063,2	K562	blood:
9	chr15:41233447..41234350-chr15:63892233..63892913,2	Hela-S3	cervix:
10	chr15:41232489..41235569-chr15:41253295..41255593,3	MCF-7	breast:
11	chr15:41233616..41234427-chr19:3534815..3535324,2	Hela-S3	cervix:
12	chr15:41233743..41234424-chr5:137799907..137800483,2	Hela-S3	cervix:
13	chr15:41130611..41132488-chr15:41231249..41233161,2	K562	blood:
14	chr15:41233583..41234336-chr5:43483972..43484531,2	Hela-S3	cervix:
15	chr15:41196058..41200363-chr15:41232746..41236796,6	MCF-7	breast:
16	chr15:41231312..41233017-chr15:41292337..41294409,2	MCF-7	breast:
17	chr15:41235426..41238056-chr15:41249028..41251261,4	MCF-7	breast:
18	chr15:41233547..41234323-chr2:32390434..32390966,2	HCT-116	colon:
19	chr15:41230478..41233329-chr15:41297882..41299703,2	MCF-7	breast:
20	chr15:41234021..41234626-chr15:41310647..41311276,2	MCF-7	breast:
21	chr15:41231280..41234394-chr15:41292861..41295820,3	K562	blood:
22	chr15:41216351..41218911-chr15:41231824..41234826,3	MCF-7	breast:
23	chr15:41233061..41238851-chr15:41242514..41246532,9	MCF-7	breast:
24	chr15:41234066..41235999-chr15:41310279..41312553,2	MCF-7	breast:
25	chr15:41233298..41234275-chr15:72978457..72979157,2	Hela-S3	cervix:
26	chr1:155947571..155948169-chr15:41233547..41234127,2	Hela-S3	cervix:
27	chr15:41201322..41202834-chr15:41232432..41234012,2	MCF-7	breast:
28	chr12:110485906..110486440-chr15:41233524..41234079,2	Hela-S3	cervix:
29	chr15:41232946..41236246-chr15:41262141..41265286,3	MCF-7	breast:
30	chr11:62609122..62610004-chr15:41233254..41234137,2	Hela-S3	cervix:
31	chr15:41221907..41222892-chr15:41234199..41234770,2	K562	blood:
32	chr15:41233383..41235115-chr15:41239344..41241397,2	MCF-7	breast:
33	chr15:41231034..41235223-chr15:41248876..41252149,4	MCF-7	breast:
34	chr15:40978878..40981252-chr15:41232643..41234691,2	MCF-7	breast:
35	chr15:41196280..41196828-chr15:41233825..41234733,2	K562	blood:
36	chr15:41193554..41195434-chr15:41232672..41235208,2	K562	blood:
37	chr15:40886274..40887836-chr15:41232537..41234993,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000174456	chromatin interactions
ENSG00000151881	chromatin interactions
ENSG00000140463	chromatin interactions
ENSG00000128965	chromatin interactions
ENSG00000152683	chromatin interactions
ENSG00000116584	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000137812	chromatin interactions
ENSG00000175202	chromatin interactions
ENSG00000259405	chromatin interactions
ENSG00000251161	chromatin interactions
ENSG00000249492	chromatin interactions
ENSG00000272716	chromatin interactions
ENSG00000196998	chromatin interactions

Extended variants
information (count: 75 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:75 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539571750	chr15:41232895-41232896	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs558326204	chr15:41232974-41232975	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs575389147	chr15:41233022-41233023	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs12442786	chr15:41233026-41233027	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs544454089	chr15:41233030-41233031	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs6492971	chr15:41233035-41233036	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs34835814	chr15:41233036-41233037	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186031847	chr15:41233061-41233062	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs138398673	chr15:41233116-41233117	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs149320365	chr15:41233123-41233124	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs532225750	chr15:41233124-41233125	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs545970721	chr15:41233135-41233136	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs113311198	chr15:41233142-41233143	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs531822982	chr15:41233145-41233146	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs548552877	chr15:41233216-41233217	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs148448834	chr15:41233252-41233253	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs76237539	chr15:41233295-41233296	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs191137903	chr15:41233311-41233312	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
19	rs530785780	chr15:41233313-41233314	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
20	rs539537102	chr15:41233318-41233319	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
21	rs550015821	chr15:41233437-41233438	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs201223262	chr15:41233531-41233532	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs368890526	chr15:41233533-41233534	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs397706052	chr15:41233535-41233536	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs568984566	chr15:41233541-41233542	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs144100157	chr15:41233544-41233545	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs7180318	chr15:41233568-41233569	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs574766292	chr15:41233581-41233582	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	Chromatin interactive region	12 gene(s)	Overlapped CNVs	n/a
29	rs369910114	chr15:41233655-41233656	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
30	rs534747900	chr15:41233712-41233713	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
31	rs551737819	chr15:41233724-41233725	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
32	rs146011214	chr15:41233762-41233763	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
33	rs112721159	chr15:41233789-41233790	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
34	rs546354733	chr15:41233798-41233799	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
35	rs529654878	chr15:41233819-41233820	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
36	rs373793641	chr15:41233874-41233875	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
37	rs562446993	chr15:41233893-41233894	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	14 gene(s)	Overlapped CNVs	n/a
38	rs576552394	chr15:41234141-41234142	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
39	rs182513390	chr15:41234174-41234175	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
40	rs112255163	chr15:41234178-41234179	Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
41	rs562342239	chr15:41234237-41234238	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	11 gene(s)	Overlapped CNVs	n/a
42	rs115987342	chr15:41234325-41234326	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs547723873	chr15:41234330-41234331	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs114606245	chr15:41234376-41234377	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Weak transcription	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs533157606	chr15:41234425-41234426	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs550217611	chr15:41234430-41234431	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs144322829	chr15:41234515-41234516	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs151031911	chr15:41234579-41234580	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs115633904	chr15:41234592-41234593	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs139699482	chr15:41234593-41234594	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17053054	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Cancer	21129771	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	21045282	CNVD
Breast cancer	22032731	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41225000-41233600	Weak transcription	Esophagus	oesophagus
2	chr15:41226000-41233000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:41226000-41233400	Weak transcription	Thymus	Thymus
4	chr15:41227800-41233600	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr15:41228000-41233200	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr15:41228600-41233600	Enhancers	Fetal Thymus	thymus
7	chr15:41229600-41233400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr15:41230000-41233000	Weak transcription	HSMMtube	muscle
9	chr15:41230000-41233400	Weak transcription	Osteobl	bone
10	chr15:41230200-41233200	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:41230200-41233200	Weak transcription	Stomach Mucosa	stomach
12	chr15:41230400-41233400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr15:41230600-41233200	Weak transcription	Fetal Heart	heart
14	chr15:41230600-41233800	Enhancers	Spleen	Spleen
15	chr15:41230800-41233000	Weak transcription	Liver	Liver
16	chr15:41230800-41233000	Weak transcription	A549	lung
17	chr15:41230800-41233600	Weak transcription	Psoas Muscle	Psoas
18	chr15:41230800-41233800	Weak transcription	Gastric	stomach
19	chr15:41231000-41233400	Enhancers	Fetal Muscle Trunk	muscle
20	chr15:41232000-41233000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:41232000-41233400	Genic enhancers	Fetal Intestine Small	intestine
22	chr15:41232000-41233400	Enhancers	Fetal Muscle Leg	muscle
23	chr15:41232000-41233600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:41232000-41233800	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
25	chr15:41232000-41234000	Enhancers	Primary B cells from peripheral blood	blood
26	chr15:41232000-41234000	Enhancers	Fetal Kidney	kidney
27	chr15:41232000-41234000	Flanking Active TSS	GM12878-XiMat	blood
28	chr15:41232200-41233000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
29	chr15:41232200-41233000	Enhancers	Lung	lung
30	chr15:41232200-41233000	Enhancers	Rectal Mucosa Donor 29	rectum
31	chr15:41232200-41233200	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
32	chr15:41232200-41233200	Enhancers	Duodenum Mucosa	Duodenum
33	chr15:41232200-41233400	Enhancers	Brain Cingulate Gyrus	brain
34	chr15:41232200-41233400	Enhancers	Right Ventricle	heart
35	chr15:41232200-41233600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr15:41232200-41233600	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr15:41232200-41233600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
38	chr15:41232400-41233000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr15:41232400-41233200	Enhancers	H9 Cell Line	embryonic stem cell
40	chr15:41232400-41233200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
41	chr15:41232400-41233200	Flanking Active TSS	Brain Hippocampus Middle	brain
42	chr15:41232400-41233200	Enhancers	Colonic Mucosa	Colon
43	chr15:41232400-41233200	Enhancers	Fetal Intestine Large	intestine
44	chr15:41232400-41233400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
45	chr15:41232400-41233400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
46	chr15:41232400-41233400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr15:41232400-41233400	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr15:41232400-41233400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
49	chr15:41232400-41233400	Enhancers	Muscle Satellite Cultured Cells	--
50	chr15:41232400-41233400	Enhancers	Brain Anterior Caudate	brain

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