Variant report

Variant	esv3397637
Chromosome Location	chr15:77991627-77993290
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:49)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:49 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr15:77992014-77992206	GM12878	blood:	n/a	n/a
2	CHD2	chr15:77991748-77992099	GM12878	blood:	n/a	n/a
3	CTCF	chr15:77991920-77992070	GM12865	blood:	n/a	n/a
4	CTCF	chr15:77991940-77992090	GM12873	blood:	n/a	n/a
5	CTCF	chr15:77991960-77992110	WERI-Rb-1	eye:	n/a	n/a
6	CTCF	chr15:77991940-77992090	GM12872	blood:	n/a	n/a
7	CTCF	chr15:77991900-77992050	HRPEpiC	eye:	n/a	n/a
8	CTCF	chr15:77991923-77992167	GM19239	blood:	n/a	n/a
9	CTCF	chr15:77991837-77991838	GM19239	blood:	n/a	n/a
10	CTCF	chr15:77992000-77992150	GM12869	blood:	n/a	n/a
11	CTCF	chr15:77991940-77992090	AG04449	skin:	n/a	n/a
12	CTCF	chr15:77991900-77992050	BE2_C	brain:	n/a	n/a
13	CTCF	chr15:77991924-77992147	MCF-7	breast:	n/a	n/a
14	CTCF	chr15:77991844-77991900	GM19239	blood:	n/a	n/a
15	ELK1	chr15:77991744-77992029	Hela-S3	cervix:	n/a	n/a
16	ELK1	chr15:77991852-77992082	GM12878	blood:	n/a	n/a
17	ESRRA	chr15:77991723-77992185	GM12878	blood:	n/a	n/a
18	GTF2F1	chr15:77991587-77992045	K562	blood:	n/a	n/a
19	GTF2F1	chr15:77991746-77992197	Hela-S3	cervix:	n/a	n/a
20	IRF3	chr15:77991926-77992099	GM12878	blood:	n/a	n/a
21	MAFK	chr15:77991724-77992133	K562	blood:	n/a	n/a
22	MAZ	chr15:77991755-77992212	Hela-S3	cervix:	n/a	n/a
23	MXI1	chr15:77991881-77992131	Hela-S3	cervix:	n/a	n/a
24	MYC	chr15:77991587-77991737	H1-hESC	embryonic stem cell:	n/a	n/a
25	MYC	chr15:77991809-77991843	MCF-7	breast:	n/a	n/a
26	MYC	chr15:77991886-77992165	MCF-7	breast:	n/a	n/a
27	MYC	chr15:77991857-77992156	MCF-7	breast:	n/a	n/a
28	MYC	chr15:77991940-77992108	HUVEC	blood vessel:	n/a	n/a
29	MYC	chr15:77991861-77991954	GM12878	blood:	n/a	n/a
30	MYC	chr15:77991836-77991840	GM12878	blood:	n/a	n/a
31	NR2C2	chr15:77991562-77992263	GM12878	blood:	n/a	n/a
32	POLR2A	chr15:77992070-77992097	Gliobla	brain:	n/a	n/a
33	POLR2A	chr15:77991996-77992044	Gliobla	brain:	n/a	n/a
34	POLR2A	chr15:77991698-77991895	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr15:77991950-77992042	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr15:77992076-77992105	ProgFib	skin:	n/a	n/a
37	POLR2A	chr15:77992079-77992103	MCF-7	breast:	n/a	n/a
38	RCOR1	chr15:77991697-77992146	K562	blood:	n/a	n/a
39	RCOR1	chr15:77991811-77992270	Hela-S3	cervix:	n/a	n/a
40	RFX5	chr15:77991895-77992209	GM12878	blood:	n/a	n/a
41	SUZ12	chr15:77991580-77992275	H1-hESC	embryonic stem cell:	n/a	n/a
42	TBP	chr15:77991751-77991926	K562	blood:	n/a	n/a
43	USF2	chr15:77991731-77992095	HepG2	liver:	n/a	n/a
44	USF2	chr15:77991763-77992037	K562	blood:	n/a	n/a
45	USF2	chr15:77991731-77991999	Hela-S3	cervix:	n/a	n/a
46	ZKSCAN1	chr15:77991744-77992166	Hela-S3	cervix:	n/a	n/a
47	ZNF143	chr15:77991737-77992218	Hela-S3	cervix:	n/a	n/a
48	ZNF263	chr15:77991579-77992664	HEK293-T-REx	kidney:	n/a	chr15:77992297-77992306 chr15:77992112-77992133 chr15:77992546-77992555
49	ZNF274	chr15:77991850-77992079	GM12878	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr15:77986790..77988861-chr15:77992181..77993938,2	K562	blood:
2	chr15:77986790..77988605-chr15:77991712..77993681,2	K562	blood:
3	chr15:77979748..77982431-chr15:77989857..77992919,3	K562	blood:
4	chr15:77988658..77990468-chr15:77993100..77994918,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMG20A-5	chr15:77991686-77991763	XLOC_011316
2	lnc-HMG20A-5	chr15:77992011-77992117	XLOC_011316
3	lnc-HMG20A-5	chr15:77991916-77991946	XLOC_011316

No data

Variant related genes	Relation type
LINGO1	TF binding region
ENSG00000169783	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201692336	chr15:77991630-77991631	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs199765478	chr15:77991638-77991639	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs74635530	chr15:77991642-77991643	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs76336815	chr15:77991650-77991651	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs78361287	chr15:77991662-77991663	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs79606535	chr15:77991664-77991665	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs79914908	chr15:77991676-77991677	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs370430616	chr15:77991680-77991681	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556490185	chr15:77991684-77991685	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs376169329	chr15:77991685-77991686	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs74715919	chr15:77991697-77991698	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs74811358	chr15:77991698-77991699	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs201937932	chr15:77991704-77991705	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs75510550	chr15:77991708-77991709	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
15	rs78963760	chr15:77991709-77991710	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
16	rs79351594	chr15:77991710-77991711	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs75940788	chr15:77991722-77991723	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
18	rs76464561	chr15:77991723-77991724	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
19	rs79754111	chr15:77991734-77991735	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
20	rs113923278	chr15:77991741-77991742	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs545195814	chr15:77991756-77991757	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
22	rs75571504	chr15:77991761-77991762	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs78539490	chr15:77991762-77991763	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs78982854	chr15:77991768-77991769	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs79938279	chr15:77991782-77991783	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs560455698	chr15:77991784-77991785	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs75893268	chr15:77991788-77991789	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs78143803	chr15:77991795-77991796	ZNF genes & repeats Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs572391059	chr15:77991800-77991801	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs80162084	chr15:77991802-77991803	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs77772428	chr15:77991805-77991806	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs77277250	chr15:77991819-77991820	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs80346626	chr15:77991821-77991822	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201015427	chr15:77991828-77991829	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs201850890	chr15:77991833-77991834	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs200096682	chr15:77991836-77991837	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs75004062	chr15:77991838-77991839	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs76567457	chr15:77991839-77991840	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs112231257	chr15:77991841-77991842	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs561306186	chr15:77991843-77991844	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs74608339	chr15:77991848-77991849	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs77836523	chr15:77991860-77991861	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs77644943	chr15:77991863-77991864	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs75041155	chr15:77991869-77991870	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs75170766	chr15:77991870-77991871	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs76604485	chr15:77991893-77991894	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs531725992	chr15:77991895-77991896	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs59511331	chr15:77991899-77991900	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs550205437	chr15:77991901-77991902	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs67486172	chr15:77991909-77991910	ZNF genes & repeats Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77969200-78007600	Weak transcription	Right Atrium	heart
2	chr15:77988600-77991800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:77989000-77991800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr15:77989000-77991800	Weak transcription	Fetal Lung	lung
5	chr15:77989800-77991800	Weak transcription	Spleen	Spleen
6	chr15:77990000-77991800	Weak transcription	Esophagus	oesophagus
7	chr15:77990400-77991800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr15:77990800-77991800	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr15:77991200-77991800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:77991600-77991800	Enhancers	Fetal Brain Female	brain
11	chr15:77991600-77991800	Bivalent/Poised TSS	NH-A	brain
12	chr15:77991600-77992200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
13	chr15:77991600-77992200	ZNF genes & repeats	Brain Angular Gyrus	brain
14	chr15:77991600-77992200	ZNF genes & repeats	Fetal Brain Male	brain
15	chr15:77991800-77992000	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
16	chr15:77991800-77992000	Bivalent/Poised TSS	Hela-S3	cervix
17	chr15:77991800-77992200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr15:77991800-77992200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr15:77991800-77992200	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
20	chr15:77991800-77992200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr15:77991800-77992200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:77991800-77992200	Bivalent/Poised TSS	Brain Anterior Caudate	brain
23	chr15:77991800-77992200	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr15:77991800-77992200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
25	chr15:77991800-77992200	ZNF genes & repeats	Brain Substantia Nigra	brain
26	chr15:77991800-77992200	ZNF genes & repeats	Colon Smooth Muscle	Colon
27	chr15:77991800-77992200	ZNF genes & repeats	Esophagus	oesophagus
28	chr15:77991800-77992200	ZNF genes & repeats	Fetal Kidney	kidney
29	chr15:77991800-77992200	ZNF genes & repeats	Fetal Lung	lung
30	chr15:77991800-77992200	Bivalent Enhancer	Fetal Stomach	stomach
31	chr15:77991800-77992200	ZNF genes & repeats	Gastric	stomach
32	chr15:77991800-77992200	ZNF genes & repeats	Lung	lung
33	chr15:77991800-77992200	ZNF genes & repeats	Pancreas	Pancrea
34	chr15:77991800-77992200	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
35	chr15:77991800-77992200	ZNF genes & repeats	Spleen	Spleen
36	chr15:77991800-77992200	Bivalent/Poised TSS	GM12878-XiMat	blood
37	chr15:77991800-77992200	ZNF genes & repeats	NHLF	lung
38	chr15:77992000-77992200	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr15:77992000-77992200	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:77992000-77992200	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
41	chr15:77992000-77992200	Bivalent Enhancer	Duodenum Smooth Muscle	Duodenum
42	chr15:77992000-77992200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
43	chr15:77992000-77992200	Bivalent/Poised TSS	Stomach Mucosa	stomach
44	chr15:77992000-77992200	Flanking Bivalent TSS/Enh	Hela-S3	cervix
45	chr15:77992000-77992200	Bivalent/Poised TSS	NHDF-Ad	bronchial
46	chr15:77992200-77993200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr15:77992200-77993600	Weak transcription	Brain Substantia Nigra	brain
48	chr15:77992200-77993600	Weak transcription	Spleen	Spleen
49	chr15:77992200-77994600	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr15:77992200-77994600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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