Variant report

Variant	esv3423388
Chromosome Location	chr15:31682185-31685233
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:368)
Chromatin interactive
region (count:2)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:31684430-31684584	K562	blood:	n/a	n/a
2	BACH1	chr15:31684087-31684895	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr15:31685217-31685417	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr15:31684196-31684858	GM12878	blood:	n/a	chr15:31684493-31684506 chr15:31684496-31684505
5	BHLHE40	chr15:31684274-31684815	K562	blood:	n/a	chr15:31684493-31684506 chr15:31684496-31684505
6	BHLHE40	chr15:31684318-31684769	HepG2	liver:	n/a	chr15:31684493-31684506 chr15:31684496-31684505
7	CCNT2	chr15:31684077-31684718	K562	blood:	n/a	chr15:31684272-31684281
8	CHD1	chr15:31683886-31684914	IMR90	lung:	n/a	chr15:31684024-31684034
9	CHD1	chr15:31684435-31684587	GM12878	blood:	n/a	n/a
10	CHD2	chr15:31684232-31684432	HepG2	liver:	n/a	n/a
11	CHD2	chr15:31684439-31684810	GM12878	blood:	n/a	n/a
12	CREB1	chr15:31684248-31684709	K562	blood:	n/a	n/a
13	CREB1	chr15:31683966-31684819	A549	lung:	n/a	n/a
14	CTBP2	chr15:31684181-31684752	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr15:31682368-31682431	GM19240	blood:	n/a	n/a
16	CTCF	chr15:31682300-31682450	HPAF	blood vessel:	n/a	n/a
17	CTCF	chr15:31682335-31682468	HepG2	liver:	n/a	n/a
18	CTCF	chr15:31682417-31682496	HepG2	liver:	n/a	n/a
19	CTCF	chr15:31684353-31684391	LNCaP	prostate:	n/a	n/a
20	CTCF	chr15:31684440-31684590	HVMF	connective:	n/a	chr15:31684562-31684575
21	CTCF	chr15:31684354-31684444	ProgFib	skin:	n/a	n/a
22	CTCF	chr15:31684618-31684620	Spleen_OC	spleen:	n/a	n/a
23	CTCF	chr15:31684300-31684450	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr15:31682300-31682450	A549	lung:	n/a	n/a
25	CTCF	chr15:31682280-31682430	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr15:31682360-31682510	HBMEC	blood vessel:	n/a	n/a
27	CTCF	chr15:31684260-31684410	WERI-Rb-1	eye:	n/a	n/a
28	CTCF	chr15:31684355-31684430	MCF-7	breast:	n/a	n/a
29	CTCF	chr15:31684320-31684470	BJ	skin:	n/a	n/a
30	CTCF	chr15:31684344-31684438	GM10248	blood:	n/a	n/a
31	CTCF	chr15:31684340-31684490	HPAF	blood vessel:	n/a	n/a
32	CTCF	chr15:31684402-31684478	GM12878	blood:	n/a	n/a
33	CTCF	chr15:31682140-31682290	GM06990	blood:	n/a	n/a
34	CTCF	chr15:31684357-31684427	MCF-7	breast:	n/a	n/a
35	CTCF	chr15:31682380-31682530	BE2_C	brain:	n/a	n/a
36	CTCF	chr15:31684300-31684450	AG04449	skin:	n/a	n/a
37	CTCF	chr15:31685160-31685310	GM12873	blood:	n/a	n/a
38	CTCF	chr15:31683960-31684110	BJ	skin:	n/a	chr15:31684022-31684035 chr15:31684022-31684035
39	CTCF	chr15:31682360-31682510	HepG2	liver:	n/a	n/a
40	CTCF	chr15:31682437-31682508	K562	blood:	n/a	n/a
41	CTCF	chr15:31684282-31684671	GM12892	blood:	n/a	chr15:31684562-31684575
42	CTCF	chr15:31684370-31684473	GM12878	blood:	n/a	n/a
43	CTCF	chr15:31684320-31684470	HMEC	breast:	n/a	n/a
44	CTCF	chr15:31684420-31684570	HCM	heart:	n/a	n/a
45	CTCF	chr15:31684562-31684598	Spleen_OC	spleen:	n/a	chr15:31684562-31684575
46	CTCF	chr15:31684260-31684410	Caco-2	colon:	n/a	n/a
47	CTCF	chr15:31684280-31684430	GM12870	blood:	n/a	n/a
48	CTCF	chr15:31684300-31684450	HRE	kidney:	n/a	n/a
49	CTCF	chr15:31684260-31684410	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr15:31684302-31684526	GM12891	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31685131-31685181	PrEC	prostate:	n/a
2	chr15:31685131-31685181	NT2-D1	testis:	n/a
3	chr15:31685131-31685181	PrEC	prostate:	n/a
4	chr15:31685131-31685181	NT2-D1	testis:	n/a
5	chr15:31684444-31684494	PrEC	prostate:	n/a
6	chr15:31684836-31684886	NB4	blood:	n/a
7	chr15:31685131-31685181	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:31684143-31684193	GM12878	blood:	n/a
9	chr15:31684836-31684886	HIPEpiC	eye:	n/a
10	chr15:31684499-31684549	Hepatocyte	liver:	n/a
11	chr15:31684143-31684193	CMK	blood:	n/a
12	chr15:31683664-31683714	T-47D	breast:	n/a
13	chr15:31685131-31685181	HAEpiC	amniotic membrane:	n/a
14	chr15:31683664-31683714	HUVEC	blood vessel:	n/a
15	chr15:31685131-31685181	HRCEpiC	kidney:	n/a
16	chr15:31684499-31684549	Jurkat	blood:	n/a
17	chr15:31684143-31684193	U87	brain:	n/a
18	chr15:31683664-31683714	HEK293	kidney:	embryo
19	chr15:31683664-31683714	A549	lung:	n/a
20	chr15:31683664-31683714	GM12892	blood:	n/a
21	chr15:31684499-31684549	Caco-2	colon:	n/a
22	chr15:31685131-31685181	BJ	skin:	n/a
23	chr15:31683664-31683714	NHDF-neo	bronchial:	n/a
24	chr15:31684143-31684193	H1-hESC	embryonic stem cell:	embryo
25	chr15:31685131-31685181	Hela-S3	cervix:	n/a
26	chr15:31683664-31683714	HAEpiC	amniotic membrane:	n/a
27	chr15:31684499-31684549	GM12878	blood:	n/a
28	chr15:31684836-31684886	MCF10A-Er-Src	breast:	n/a
29	chr15:31684499-31684549	GM19239	blood:	n/a
30	chr15:31684836-31684886	RPTEC	kidney:	n/a
31	chr15:31684499-31684549	CMK	blood:	n/a
32	chr15:31684836-31684886	AG04449	skin:	fetal
33	chr15:31684143-31684193	HCF	heart:	n/a
34	chr15:31685131-31685181	NHBE	bronchial:	n/a
35	chr15:31684444-31684494	T-47D	breast:	n/a
36	chr15:31684836-31684886	LNCaP	prostate:	n/a
37	chr15:31684499-31684549	HCT-116	colon:	n/a
38	chr15:31684444-31684494	HRE	kidney:	n/a
39	chr15:31685131-31685181	MCF10A-Er-Src	breast:	n/a
40	chr15:31684499-31684549	HL-60	blood:	n/a
41	chr15:31684444-31684494	HCT-116	colon:	n/a
42	chr15:31684143-31684193	HepG2	liver:	n/a
43	chr15:31684444-31684494	PFSK-1	brain:	n/a
44	chr15:31684143-31684193	SKMC	muscle:	n/a
45	chr15:31684143-31684193	NHDF-neo	bronchial:	n/a
46	chr15:31685131-31685181	HNPCEpiC	eye:	n/a
47	chr15:31684836-31684886	HRE	kidney:	n/a
48	chr15:31684143-31684193	NB4	blood:	n/a
49	chr15:31684836-31684886	Jurkat	blood:	n/a
50	chr15:31684499-31684549	K562	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:31682078..31683956-chr15:31730554..31733122,2	K562	blood:
2	chr15:31616992..31619470-chr15:31682984..31685911,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAN1-2	chr15:31685046-31685458	NONHSAT140225
2	lnc-FAN1-2	chr15:31685046-31685458	ENSG00000246638
3	lnc-FAN1-2	chr15:31685046-31685458	XLOC_011202
4	lnc-FAN1-2	chr15:31685046-31685458	XLOC_011202

No data

Variant related genes	Relation type
KLF13	TF binding region
KLF13	CpG island
ENSG00000169926	chromatin interactions
RRM2	miRNA target sites
FAM135A	miRNA target sites

Extended variants
information (count: 100 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs557053640	chr15:31682188-31682189	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs576714932	chr15:31682297-31682298	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs72722847	chr15:31682346-31682347	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs559219249	chr15:31682375-31682376	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs12912800	chr15:31682376-31682377	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs144833585	chr15:31682403-31682404	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs561126271	chr15:31682412-31682413	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs530175300	chr15:31682418-31682419	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs28664837	chr15:31682469-31682470	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs543521504	chr15:31682507-31682508	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs572441346	chr15:31682541-31682542	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs532189114	chr15:31682574-31682575	Weak transcription ZNF genes & repeats Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs552068802	chr15:31682612-31682613	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs536239809	chr15:31682632-31682633	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs565990639	chr15:31682686-31682687	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs528371086	chr15:31682689-31682690	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs548208512	chr15:31682697-31682698	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs34667526	chr15:31682700-31682701	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs568070586	chr15:31682730-31682731	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs536997597	chr15:31682739-31682740	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs182490048	chr15:31682776-31682777	ZNF genes & repeats Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs148587974	chr15:31682831-31682832	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs570530201	chr15:31682856-31682857	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs539256648	chr15:31682883-31682884	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs116487606	chr15:31682921-31682922	Weak transcription Bivalent Enhancer Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs34682798	chr15:31682926-31682927	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs77611231	chr15:31682953-31682954	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs142898294	chr15:31682982-31682983	Weak transcription Bivalent Enhancer Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574512972	chr15:31683054-31683055	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs543376708	chr15:31683063-31683064	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs74519566	chr15:31683069-31683070	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs151095707	chr15:31683206-31683207	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs142395036	chr15:31683249-31683250	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs12440241	chr15:31683334-31683335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs59970767	chr15:31683369-31683370	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs369991014	chr15:31683459-31683460	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs187860705	chr15:31683559-31683560	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs528246930	chr15:31683600-31683601	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs372237956	chr15:31683617-31683618	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs8030297	chr15:31683624-31683625	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs8025401	chr15:31683694-31683695	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs192627325	chr15:31683740-31683741	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs185083065	chr15:31683789-31683790	Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs190327143	chr15:31683822-31683823	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs530537511	chr15:31683829-31683830	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs550580310	chr15:31683833-31683834	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570589436	chr15:31683883-31683884	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs539159199	chr15:31683888-31683889	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs71422888	chr15:31683925-31683926	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559779986	chr15:31683967-31683968	Weak transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:90)

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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Pancreatic cancer	17952125	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD

Chromatin state (count:384 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31670800-31683800	Weak transcription	Small Intestine	intestine
2	chr15:31673600-31684000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr15:31674200-31684000	Weak transcription	Colonic Mucosa	Colon
4	chr15:31674600-31683800	Weak transcription	Primary B cells from peripheral blood	blood
5	chr15:31674600-31684000	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr15:31675000-31684000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr15:31675200-31684000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr15:31675800-31683800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr15:31675800-31683800	Weak transcription	Right Atrium	heart
10	chr15:31675800-31684000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr15:31676600-31683000	Weak transcription	Fetal Intestine Large	intestine
12	chr15:31677000-31683400	Enhancers	Primary T helper cells fromperipheralblood	blood
13	chr15:31677000-31684000	Weak transcription	Gastric	stomach
14	chr15:31679400-31682200	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr15:31680200-31683600	Weak transcription	Right Ventricle	heart
16	chr15:31680400-31682200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr15:31680400-31682800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr15:31680400-31683000	Weak transcription	Lung	lung
19	chr15:31680400-31683600	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr15:31680400-31683800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr15:31680400-31683800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr15:31680400-31684000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr15:31680400-31684000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr15:31680400-31684000	Enhancers	Primary T cells fromperipheralblood	blood
25	chr15:31680400-31684000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:31680400-31684000	Weak transcription	Brain Anterior Caudate	brain
27	chr15:31680400-31684000	Weak transcription	Brain Inferior Temporal Lobe	brain
28	chr15:31680400-31684000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr15:31680400-31684000	Weak transcription	Brain Substantia Nigra	brain
30	chr15:31680400-31684000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr15:31680400-31684000	Weak transcription	Esophagus	oesophagus
32	chr15:31680400-31684200	Weak transcription	Spleen	Spleen
33	chr15:31680600-31683800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr15:31680600-31684000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr15:31680600-31684000	Weak transcription	Liver	Liver
36	chr15:31680600-31684000	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr15:31680600-31684000	Weak transcription	Rectal Smooth Muscle	rectum
38	chr15:31680600-31684000	Weak transcription	GM12878-XiMat	blood
39	chr15:31680600-31684000	Weak transcription	Hela-S3	cervix
40	chr15:31680800-31682800	Weak transcription	Fetal Heart	heart
41	chr15:31680800-31684000	Weak transcription	Primary T cells from cord blood	blood
42	chr15:31680800-31684000	Weak transcription	Pancreas	Pancrea
43	chr15:31680800-31684000	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr15:31680800-31684000	Weak transcription	Stomach Smooth Muscle	stomach
45	chr15:31680800-31684000	Weak transcription	HMEC	breast
46	chr15:31680800-31684000	Weak transcription	Osteobl	bone
47	chr15:31680800-31684200	Weak transcription	Dnd41	blood
48	chr15:31681200-31682600	Weak transcription	Primary T helper cells PMA-I stimulated	--
49	chr15:31681200-31684000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr15:31681400-31683200	Enhancers	Primary T killer naive cells fromperipheralblood	blood

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