Variant report

Variant	esv3357816
Chromosome Location	chr20:25448102-25451400
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	ATF1	chr20:25450740-25450940	K562	blood:	n/a	n/a
2	BHLHE40	chr20:25450555-25450968	K562	blood:	n/a	n/a
3	BRCA1	chr20:25450882-25450972	HepG2	liver:	n/a	n/a
4	CHD2	chr20:25450756-25450757	HepG2	liver:	n/a	n/a
5	CREB1	chr20:25450697-25451039	A549	lung:	n/a	n/a
6	CTCF	chr20:25450748-25450961	GM20000	blood:	n/a	chr20:25450843-25450856
7	CTCF	chr20:25450763-25450975	A549	lung:	n/a	chr20:25450843-25450856
8	CTCF	chr20:25450651-25451055	GM12878	blood:	n/a	chr20:25450843-25450856
9	CTCF	chr20:25450800-25450950	HMEC	breast:	n/a	chr20:25450843-25450856
10	CTCF	chr20:25450453-25451214	SK-N-SH	brain:	n/a	chr20:25450843-25450856
11	CTCF	chr20:25450743-25450946	HUVEC	blood vessel:	n/a	chr20:25450843-25450856
12	CTCF	chr20:25450780-25450930	HMEC	breast:	n/a	chr20:25450843-25450856
13	CTCF	chr20:25450724-25450973	MCF-7	breast:	n/a	chr20:25450843-25450856
14	CTCF	chr20:25450800-25450950	HA-sp	spinal cord:	n/a	chr20:25450843-25450856
15	CTCF	chr20:25450760-25450910	BJ	skin:	n/a	chr20:25450843-25450856
16	CTCF	chr20:25450780-25450930	HepG2	liver:	n/a	chr20:25450843-25450856
17	CTCF	chr20:25450800-25450950	BE2_C	brain:	n/a	chr20:25450843-25450856
18	CTCF	chr20:25450760-25450910	NHDF-neo	bronchial:	n/a	chr20:25450843-25450856
19	CTCF	chr20:25450716-25451037	A549	lung:	n/a	chr20:25450843-25450856
20	CTCF	chr20:25450760-25450910	HEEpiC	esophagus:	n/a	chr20:25450843-25450856
21	CTCF	chr20:25450780-25450930	AG04449	skin:	n/a	chr20:25450843-25450856
22	CTCF	chr20:25450703-25450984	H1-hESC	embryonic stem cell:	n/a	chr20:25450843-25450856
23	CTCF	chr20:25450760-25450910	RPTEC	kidney:	n/a	chr20:25450843-25450856
24	CTCF	chr20:25450685-25451175	MCF-7	breast:	n/a	chr20:25450843-25450856
25	CTCF	chr20:25450751-25450951	GM10248	blood:	n/a	chr20:25450843-25450856
26	CTCF	chr20:25450737-25450995	A549	lung:	n/a	chr20:25450843-25450856
27	CTCF	chr20:25450742-25450902	SK-N-SH_RA	brain:	n/a	chr20:25450843-25450856
28	CTCF	chr20:25450780-25450930	HRE	kidney:	n/a	chr20:25450843-25450856
29	CTCF	chr20:25450660-25450810	HAc	cerebellar:	n/a	n/a
30	CTCF	chr20:25450752-25450944	GM13976	blood:	n/a	chr20:25450843-25450856
31	CTCF	chr20:25450780-25450930	GM12869	blood:	n/a	chr20:25450843-25450856
32	CTCF	chr20:25450740-25450890	HVMF	connective:	n/a	chr20:25450843-25450856
33	CTCF	chr20:25450730-25450975	HepG2	liver:	n/a	chr20:25450843-25450856
34	CTCF	chr20:25450820-25450970	HVMF	connective:	n/a	chr20:25450843-25450856
35	CTCF	chr20:25450760-25450910	HEK293	kidney:	n/a	chr20:25450843-25450856
36	CTCF	chr20:25450693-25450995	GM19238	blood:	n/a	chr20:25450843-25450856
37	CTCF	chr20:25450780-25450930	AG10803	skin:	n/a	chr20:25450843-25450856
38	CTCF	chr20:25450536-25450585	GM19238	blood:	n/a	n/a
39	CTCF	chr20:25450713-25450979	MCF-7	breast:	n/a	chr20:25450843-25450856
40	CTCF	chr20:25450780-25450930	HFF-Myc	foreskin:	n/a	chr20:25450843-25450856
41	CTCF	chr20:25450760-25450910	HCPEpiC	choroid plexus:	n/a	chr20:25450843-25450856
42	CTCF	chr20:25450780-25450930	Hela-S3	cervix:	n/a	chr20:25450843-25450856
43	CTCF	chr20:25450780-25450930	HCFaa	heart:	n/a	chr20:25450843-25450856
44	CTCF	chr20:25450723-25450978	GM13977	blood:	n/a	chr20:25450843-25450856
45	CTCF	chr20:25450760-25450910	HRPEpiC	eye:	n/a	chr20:25450843-25450856
46	CTCF	chr20:25450706-25450992	GM19240	blood:	n/a	chr20:25450843-25450856
47	CTCF	chr20:25450760-25450910	K562	blood:	n/a	chr20:25450843-25450856
48	CTCF	chr20:25450780-25450930	HCPEpiC	choroid plexus:	n/a	chr20:25450843-25450856
49	CTCF	chr20:25450800-25450950	NHLF	lung:	n/a	chr20:25450843-25450856
50	CTCF	chr20:25450666-25451066	K562	blood:	n/a	chr20:25450843-25450856

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:25448861-25448911	SK-N-SH	brain:	n/a
2	chr20:25450839-25450889	AG10803	skin:	n/a
3	chr20:25448861-25448911	GM12878	blood:	n/a
4	chr20:25448861-25448911	HPAEpiC	pulmonary alveolar:	n/a
5	chr20:25450839-25450889	PFSK-1	brain:	n/a
6	chr20:25450839-25450889	NT2-D1	testis:	n/a
7	chr20:25448861-25448911	ECC-1	luminal epithelium:	n/a
8	chr20:25448861-25448911	HUVEC	blood vessel:	n/a
9	chr20:25450839-25450889	SAEC	small airway:	n/a
10	chr20:25450839-25450889	HPAEpiC	pulmonary alveolar:	n/a
11	chr20:25448861-25448911	HRCEpiC	kidney:	n/a
12	chr20:25450839-25450889	GM12878	blood:	n/a
13	chr20:25448861-25448911	NH-A	brain:	n/a
14	chr20:25450839-25450889	ECC-1	luminal epithelium:	n/a
15	chr20:25450839-25450889	HEEpiC	esophagus:	n/a
16	chr20:25450839-25450889	HL-60	blood:	n/a
17	chr20:25448861-25448911	AG09309	skin:	n/a
18	chr20:25450839-25450889	PANC-1	pancreas:	n/a
19	chr20:25450839-25450889	GM12892	blood:	n/a
20	chr20:25448861-25448911	HEEpiC	esophagus:	n/a
21	chr20:25450839-25450889	AG09309	skin:	n/a
22	chr20:25448861-25448911	H1-hESC	embryonic stem cell:	embryo
23	chr20:25448861-25448911	HL-60	blood:	n/a
24	chr20:25448861-25448911	HCM	heart:	n/a
25	chr20:25448861-25448911	PFSK-1	brain:	n/a
26	chr20:25448861-25448911	AG04450	lung:	fetal
27	chr20:25450839-25450889	SK-N-SH_RA	brain:	n/a
28	chr20:25450839-25450889	HCM	heart:	n/a
29	chr20:25450839-25450889	HRE	kidney:	n/a
30	chr20:25448861-25448911	AG04449	skin:	fetal
31	chr20:25448861-25448911	HCT-116	colon:	n/a
32	chr20:25450839-25450889	RPTEC	kidney:	n/a
33	chr20:25448861-25448911	T-47D	breast:	n/a
34	chr20:25448861-25448911	GM12891	blood:	n/a
35	chr20:25450839-25450889	T-47D	breast:	n/a
36	chr20:25448861-25448911	Caco-2	colon:	n/a
37	chr20:25448861-25448911	GM19239	blood:	n/a
38	chr20:25450839-25450889	HIPEpiC	eye:	n/a
39	chr20:25448861-25448911	K562	blood:	n/a
40	chr20:25448861-25448911	Hela-S3	cervix:	n/a
41	chr20:25448861-25448911	AoSMC	blood vessel:	n/a
42	chr20:25448861-25448911	HRPEpiC	eye:	n/a
43	chr20:25448861-25448911	HepG2	liver:	n/a
44	chr20:25450839-25450889	SKMC	muscle:	n/a
45	chr20:25448861-25448911	HEK293	kidney:	embryo
46	chr20:25450839-25450889	GM06990	blood:	n/a
47	chr20:25448861-25448911	HMEC	breast:	n/a
48	chr20:25448861-25448911	LNCaP	prostate:	n/a
49	chr20:25450839-25450889	ovcar-3	ovarian:	n/a
50	chr20:25450839-25450889	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:59433764..59435297-chr20:25448424..25451207,2	MCF-7	breast:
2	chr20:25450464..25451286-chr20:25554579..25555594,4	MCF-7	breast:
3	chr20:25445981..25448619-chr20:25473407..25476003,2	K562	blood:
4	chr20:25450369..25451319-chr20:25554838..25555706,2	K562	blood:

Variant related genes	Relation type
NINL	TF binding region
NINL	CpG island

Extended variants
information (count: 169 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:169 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111331913	chr20:25448119-25448120	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs193264975	chr20:25448123-25448124	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138839711	chr20:25448138-25448139	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs56795563	chr20:25448153-25448154	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs142787484	chr20:25448191-25448192	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs530334116	chr20:25448207-25448208	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs77136063	chr20:25448256-25448257	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs116542575	chr20:25448276-25448277	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543690396	chr20:25448283-25448284	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs559971344	chr20:25448308-25448309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs374203967	chr20:25448311-25448312	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185389040	chr20:25448335-25448336	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs144633399	chr20:25448353-25448354	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs151115848	chr20:25448376-25448377	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs188758497	chr20:25448383-25448384	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550558787	chr20:25448406-25448407	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs560973997	chr20:25448441-25448442	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs570992745	chr20:25448444-25448445	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs34897953	chr20:25448454-25448455	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs530117132	chr20:25448468-25448469	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs59362331	chr20:25448493-25448494	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs113578449	chr20:25448546-25448547	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs566629971	chr20:25448609-25448610	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs368116462	chr20:25448671-25448672	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532207748	chr20:25448675-25448676	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552405562	chr20:25448712-25448713	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191946449	chr20:25448738-25448739	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538188463	chr20:25448834-25448835	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs199720330	chr20:25448846-25448847	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs200352239	chr20:25448849-25448850	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs554585535	chr20:25448862-25448863	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs74526598	chr20:25448873-25448874	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs568099098	chr20:25448890-25448891	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs370610108	chr20:25448904-25448905	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs533839410	chr20:25448940-25448941	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553932135	chr20:25448942-25448943	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs184114196	chr20:25449106-25449107	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375675347	chr20:25449127-25449128	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs545282405	chr20:25449164-25449165	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs142756060	chr20:25449170-25449171	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs56352955	chr20:25449172-25449173	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs378240	chr20:25449174-25449175	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
43	rs575826391	chr20:25449179-25449180	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs188464546	chr20:25449195-25449196	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368273502	chr20:25449307-25449308	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs560910720	chr20:25449335-25449336	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530057053	chr20:25449389-25449390	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs181021120	chr20:25449392-25449393	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs58238985	chr20:25449417-25449418	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs527452852	chr20:25449431-25449432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Oral cancer	21386901	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25425600-25453200	Weak transcription	Small Intestine	intestine
2	chr20:25426400-25450200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr20:25427200-25488200	Weak transcription	Stomach Mucosa	stomach
4	chr20:25429400-25463200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr20:25429800-25458800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr20:25430200-25484400	Strong transcription	Fetal Stomach	stomach
7	chr20:25431800-25484200	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr20:25432400-25450400	Strong transcription	Thymus	Thymus
9	chr20:25432600-25452400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
10	chr20:25434400-25460800	Weak transcription	Fetal Heart	heart
11	chr20:25435600-25459000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr20:25435800-25450200	Weak transcription	Fetal Kidney	kidney
13	chr20:25435800-25465600	Weak transcription	NH-A	brain
14	chr20:25436000-25448200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr20:25436200-25465200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr20:25437800-25454600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr20:25438000-25450800	Strong transcription	Dnd41	blood
18	chr20:25438000-25452600	Strong transcription	Brain Germinal Matrix	brain
19	chr20:25438000-25456400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr20:25438200-25449200	Strong transcription	Liver	Liver
21	chr20:25438200-25449400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr20:25438200-25450200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
23	chr20:25438200-25452400	Strong transcription	Fetal Brain Female	brain
24	chr20:25438400-25449000	Strong transcription	H9 Cell Line	embryonic stem cell
25	chr20:25438400-25451800	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr20:25438400-25452600	Strong transcription	Ovary	ovary
27	chr20:25438400-25455400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr20:25438600-25448800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr20:25438600-25451800	Strong transcription	Stomach Smooth Muscle	stomach
30	chr20:25438600-25453200	Strong transcription	Fetal Intestine Small	intestine
31	chr20:25438600-25466200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr20:25438800-25449200	Strong transcription	HUES6 Cell Line	embryonic stem cell
33	chr20:25438800-25455000	Strong transcription	Fetal Intestine Large	intestine
34	chr20:25438800-25472600	Strong transcription	HepG2	liver
35	chr20:25440600-25466600	Weak transcription	Left Ventricle	heart
36	chr20:25441000-25452200	Strong transcription	A549	lung
37	chr20:25441200-25450200	Weak transcription	Colonic Mucosa	Colon
38	chr20:25441200-25450600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr20:25441800-25449000	Strong transcription	H1 Cell Line	embryonic stem cell
40	chr20:25441800-25449400	Strong transcription	HUES64 Cell Line	embryonic stem cell
41	chr20:25441800-25455000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
42	chr20:25442200-25460000	Weak transcription	Brain Angular Gyrus	brain
43	chr20:25442800-25450800	Weak transcription	Osteobl	bone
44	chr20:25443200-25459000	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr20:25443800-25457400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
46	chr20:25444000-25448600	Strong transcription	Fetal Lung	lung
47	chr20:25444000-25452000	Strong transcription	HUES48 Cell Line	embryonic stem cell
48	chr20:25444200-25452600	Strong transcription	Duodenum Smooth Muscle	Duodenum
49	chr20:25444400-25450400	Strong transcription	iPS-15b Cell Line	embryonic stem cell
50	chr20:25445000-25451400	Strong transcription	Gastric	stomach

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