Variant report

Variant	nsv436201
Chromosome Location	chr15:42380264-42387429
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:42384291-42384424	HepG2	liver:	n/a	n/a
2	BATF	chr15:42384572-42384862	GM12878	blood:	n/a	n/a
3	BATF	chr15:42384559-42384843	GM12878	blood:	n/a	n/a
4	BHLHE40	chr15:42383963-42384237	K562	blood:	n/a	n/a
5	BHLHE40	chr15:42383934-42384302	HepG2	liver:	n/a	n/a
6	BHLHE40	chr15:42384095-42384135	GM12878	blood:	n/a	n/a
7	BHLHE40	chr15:42382943-42383191	K562	blood:	n/a	n/a
8	BRCA1	chr15:42384578-42384896	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr15:42384452-42384932	Hela-S3	cervix:	n/a	chr15:42384550-42384562
10	CHD2	chr15:42384582-42384950	Hela-S3	cervix:	n/a	n/a
11	CTCF	chr15:42386792-42387084	MCF-7	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
12	CTCF	chr15:42386860-42387010	Hela-S3	cervix:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
13	CTCF	chr15:42386835-42387067	MCF-7	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
14	CTCF	chr15:42386840-42386990	GM12865	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
15	CTCF	chr15:42383495-42383884	K562	blood:	n/a	n/a
16	CTCF	chr15:42384080-42384230	HepG2	liver:	n/a	n/a
17	CTCF	chr15:42386604-42387195	HCT-116	colon:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
18	CTCF	chr15:42386820-42386970	HMEC	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
19	CTCF	chr15:42386760-42386910	HCT-116	colon:	n/a	chr15:42386900-42386908
20	CTCF	chr15:42386860-42387010	MCF-7	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
21	CTCF	chr15:42386860-42387010	SAEC	small airway:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
22	CTCF	chr15:42386710-42387212	MCF-7	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
23	CTCF	chr15:42386950-42386969	Hela-S3	cervix:	n/a	chr15:42386954-42386967
24	CTCF	chr15:42386740-42386890	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr15:42386744-42387129	HepG2	liver:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
26	CTCF	chr15:42386880-42387030	GM12878	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
27	CTCF	chr15:42386759-42387005	K562	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
28	CTCF	chr15:42386820-42386970	WERI-Rb-1	eye:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
29	CTCF	chr15:42383469-42383724	K562	blood:	n/a	n/a
30	CTCF	chr15:42386878-42387033	GM12892	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
31	CTCF	chr15:42386786-42387032	K562	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
32	CTCF	chr15:42386852-42386998	Pancreas_OC	pancreas:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
33	CTCF	chr15:42383646-42383728	K562	blood:	n/a	n/a
34	CTCF	chr15:42386880-42387030	GM12872	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
35	CTCF	chr15:42386949-42386998	GM19239	blood:	n/a	chr15:42386954-42386967
36	CTCF	chr15:42386860-42387010	NHEK	skin:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
37	CTCF	chr15:42386900-42387050	HMEC	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
38	CTCF	chr15:42386836-42387069	NHEK	skin:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
39	CTCF	chr15:42386860-42387010	HEEpiC	esophagus:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
40	CTCF	chr15:42386840-42386990	HepG2	liver:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
41	CTCF	chr15:42386676-42387257	MCF-7	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
42	CTCF	chr15:42386791-42387025	HepG2	liver:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
43	CTCF	chr15:42386787-42387124	GM12878	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
44	CTCF	chr15:42386980-42387130	GM12871	blood:	n/a	n/a
45	CTCF	chr15:42386821-42387084	MCF-7	breast:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
46	CTCF	chr15:42386920-42387070	BE2_C	brain:	n/a	chr15:42386954-42386967
47	CTCF	chr15:42383480-42383776	K562	blood:	n/a	n/a
48	CTCF	chr15:42386785-42387080	K562	blood:	n/a	chr15:42386954-42386967 chr15:42386900-42386908
49	CTCF	chr15:42386935-42387013	H1-hESC	embryonic stem cell:	n/a	chr15:42386954-42386967
50	CTCF	chr15:42386908-42386986	K562	blood:	n/a	chr15:42386954-42386967

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:42386816-42386866	NH-A	brain:	n/a
2	chr15:42387193-42387243	MCF-7	breast:	n/a
3	chr15:42386816-42386866	NH-A	brain:	n/a
4	chr15:42387193-42387243	MCF-7	breast:	n/a
5	chr15:42386909-42386959	SK-N-SH	brain:	n/a
6	chr15:42386909-42386959	AG10803	skin:	n/a
7	chr15:42387193-42387243	HepG2	liver:	n/a
8	chr15:42386726-42386776	PrEC	prostate:	n/a
9	chr15:42386816-42386866	HIPEpiC	eye:	n/a
10	chr15:42386726-42386776	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:42387193-42387243	HEEpiC	esophagus:	n/a
12	chr15:42387193-42387243	NHDF-neo	bronchial:	n/a
13	chr15:42387193-42387243	AG09309	skin:	n/a
14	chr15:42386816-42386866	MCF10A-Er-Src	breast:	n/a
15	chr15:42386816-42386866	SAEC	small airway:	n/a
16	chr15:42387287-42387337	HAEpiC	amniotic membrane:	n/a
17	chr15:42387287-42387337	GM12892	blood:	n/a
18	chr15:42387287-42387337	HRE	kidney:	n/a
19	chr15:42387193-42387243	HNPCEpiC	eye:	n/a
20	chr15:42386726-42386776	MCF-7	breast:	n/a
21	chr15:42386726-42386776	NB4	blood:	n/a
22	chr15:42387193-42387243	K562	blood:	n/a
23	chr15:42386909-42386959	H1-hESC	embryonic stem cell:	embryo
24	chr15:42387193-42387243	GM12892	blood:	n/a
25	chr15:42387287-42387337	AG09319	gingival:	n/a
26	chr15:42387193-42387243	ECC-1	luminal epithelium:	n/a
27	chr15:42386726-42386776	H1-hESC	embryonic stem cell:	embryo
28	chr15:42387287-42387337	SK-N-MC	brain:	n/a
29	chr15:42387193-42387243	A549	lung:	n/a
30	chr15:42386726-42386776	GM12891	blood:	n/a
31	chr15:42386909-42386959	NB4	blood:	n/a
32	chr15:42387193-42387243	NB4	blood:	n/a
33	chr15:42386726-42386776	AG09319	gingival:	n/a
34	chr15:42387287-42387337	CMK	blood:	n/a
35	chr15:42387193-42387243	SK-N-MC	brain:	n/a
36	chr15:42386909-42386959	HRCEpiC	kidney:	n/a
37	chr15:42386909-42386959	U87	brain:	n/a
38	chr15:42386816-42386866	SK-N-SH_RA	brain:	n/a
39	chr15:42386726-42386776	HNPCEpiC	eye:	n/a
40	chr15:42387287-42387337	GM12878	blood:	n/a
41	chr15:42386816-42386866	CMK	blood:	n/a
42	chr15:42386909-42386959	HEEpiC	esophagus:	n/a
43	chr15:42387287-42387337	PANC-1	pancreas:	n/a
44	chr15:42386726-42386776	HIPEpiC	eye:	n/a
45	chr15:42386909-42386959	GM12891	blood:	n/a
46	chr15:42386816-42386866	NT2-D1	testis:	n/a
47	chr15:42386726-42386776	BJ	skin:	n/a
48	chr15:42386726-42386776	AG04450	lung:	fetal
49	chr15:42387193-42387243	RPTEC	kidney:	n/a
50	chr15:42386816-42386866	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:42370010..42372757-chr15:42379600..42382035,2	K562	blood:
2	chr15:42374455..42376653-chr15:42378778..42380758,2	K562	blood:
3	chr15:42384743..42386720-chr15:42391434..42393196,2	MCF-7	breast:
4	chr15:42363019..42364718-chr15:42379292..42382030,2	K562	blood:
5	chr15:42378120..42380874-chr15:42393384..42396333,2	K562	blood:

Variant related genes	Relation type
PLA2G4D	TF binding region
PLA2G4D	CpG island
ENSG00000159337	chromatin interactions

Extended variants
information (count: 335 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:335 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114489018	chr15:42380339-42380340	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs530829424	chr15:42380341-42380342	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs550530739	chr15:42380349-42380350	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs188464630	chr15:42380356-42380357	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529761410	chr15:42380384-42380385	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs776726	chr15:42380395-42380396	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs566142809	chr15:42380415-42380416	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs4924620	chr15:42380429-42380430	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs117799515	chr15:42380448-42380449	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs569480249	chr15:42380632-42380633	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369256043	chr15:42380636-42380637	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548960275	chr15:42380641-42380642	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs554882307	chr15:42380651-42380652	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs575054998	chr15:42380662-42380663	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs35375357	chr15:42380670-42380671	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs534372081	chr15:42380705-42380706	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs559091795	chr15:42380720-42380721	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs534289615	chr15:42380727-42380728	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs76838799	chr15:42380731-42380732	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs74647964	chr15:42380732-42380733	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs554266665	chr15:42380763-42380764	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs577405598	chr15:42380775-42380776	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs17748059	chr15:42380802-42380803	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs562878674	chr15:42380821-42380822	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs112319774	chr15:42380824-42380825	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs544468220	chr15:42380937-42380938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs560752416	chr15:42380955-42380956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs528073043	chr15:42380965-42380966	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567578148	chr15:42380990-42380991	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs181655869	chr15:42381016-42381017	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs546382005	chr15:42381019-42381020	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559863854	chr15:42381022-42381023	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532214985	chr15:42381070-42381071	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551923693	chr15:42381087-42381088	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs185247259	chr15:42381096-42381097	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs538175047	chr15:42381142-42381143	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs548850438	chr15:42381143-42381144	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs568677173	chr15:42381148-42381149	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs9920766	chr15:42381191-42381192	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs7176443	chr15:42381196-42381197	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs7176459	chr15:42381215-42381216	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs190575154	chr15:42381235-42381236	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs639560	chr15:42381240-42381241	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs553802963	chr15:42381246-42381247	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs576338978	chr15:42381278-42381279	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182417880	chr15:42381284-42381285	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554484544	chr15:42381291-42381292	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187027391	chr15:42381293-42381294	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs540067188	chr15:42381321-42381322	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs149989584	chr15:42381322-42381323	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:69)

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
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
Myelofibrosis	22110671	CNVD
Maculopathy	20981449	CNVD
Gastric adenocarcinoma	19115996	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:180 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:42369800-42385000	Weak transcription	Right Atrium	heart
2	chr15:42371800-42380800	Weak transcription	Pancreas	Pancrea
3	chr15:42372800-42383000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr15:42373400-42384400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr15:42373400-42384400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:42376800-42384400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:42377000-42381000	Weak transcription	Fetal Heart	heart
8	chr15:42377200-42381200	Weak transcription	Primary hematopoietic stem cells	blood
9	chr15:42377400-42381000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr15:42377400-42382400	Weak transcription	Fetal Intestine Large	intestine
11	chr15:42377400-42384800	Weak transcription	Esophagus	oesophagus
12	chr15:42377600-42380800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr15:42377600-42381000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr15:42377600-42381400	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr15:42377600-42383000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr15:42377600-42384800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:42377800-42382400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr15:42377800-42384200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr15:42378000-42381600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr15:42378000-42382400	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr15:42378000-42382400	Weak transcription	NHEK	skin
22	chr15:42378200-42382600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr15:42378200-42382600	Weak transcription	HMEC	breast
24	chr15:42378200-42384800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr15:42378600-42380800	Weak transcription	Fetal Thymus	thymus
26	chr15:42380000-42381400	Enhancers	Hela-S3	cervix
27	chr15:42380000-42383000	Enhancers	Stomach Mucosa	stomach
28	chr15:42380200-42380400	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr15:42380200-42381600	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr15:42380200-42383000	Enhancers	Gastric	stomach
31	chr15:42380600-42380800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:42380600-42380800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
33	chr15:42380800-42381600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr15:42380800-42381600	Enhancers	Fetal Thymus	thymus
35	chr15:42380800-42382200	Enhancers	Pancreas	Pancrea
36	chr15:42381000-42381200	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr15:42381000-42381800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr15:42381000-42382200	Enhancers	Fetal Heart	heart
39	chr15:42381000-42382800	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr15:42381000-42383000	Enhancers	Colonic Mucosa	Colon
41	chr15:42381000-42383000	Enhancers	Duodenum Mucosa	Duodenum
42	chr15:42381000-42383400	Bivalent Enhancer	HepG2	liver
43	chr15:42381200-42381800	Enhancers	Primary hematopoietic stem cells	blood
44	chr15:42381400-42381600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr15:42381400-42381600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr15:42381400-42381800	Enhancers	Right Ventricle	heart
47	chr15:42381400-42382000	Enhancers	Left Ventricle	heart
48	chr15:42381400-42382600	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr15:42381600-42381800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr15:42381600-42382600	Weak transcription	Rectal Mucosa Donor 29	rectum

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