Variant report

Variant	esv3420486
Chromosome Location	chr8:124661471-124665669
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:7)
CpG islands
(count:183)
Chromatin interactive
region (count:5)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:7 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr8:124663960-124664110	GM12875	blood:	n/a	n/a
2	CTCF	chr8:124664120-124664270	GM12875	blood:	n/a	n/a
3	CUX1	chr8:124665397-124665635	K562	blood:	n/a	n/a
4	EBF1	chr8:124662985-124663302	GM12878	blood:	n/a	chr8:124663181-124663192 chr8:124663180-124663193
5	MXI1	chr8:124665458-124666702	IMR90	lung:	n/a	n/a
6	MYC	chr8:124665459-124665497	NB4	blood:	n/a	n/a
7	SUZ12	chr8:124663436-124663643	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:124665016-124665066	U87	brain:	n/a
2	chr8:124665021-124665071	NT2-D1	testis:	n/a
3	chr8:124665021-124665071	HRE	kidney:	n/a
4	chr8:124665021-124665071	GM19239	blood:	n/a
5	chr8:124665021-124665071	A549	lung:	n/a
6	chr8:124665293-124665343	Caco-2	colon:	n/a
7	chr8:124665293-124665343	GM12892	blood:	n/a
8	chr8:124665293-124665343	Jurkat	blood:	n/a
9	chr8:124665016-124665066	SK-N-MC	brain:	n/a
10	chr8:124665021-124665071	HEK293	kidney:	embryo
11	chr8:124665293-124665343	HCF	heart:	n/a
12	chr8:124665016-124665066	ProgFib	skin:	n/a
13	chr8:124665016-124665066	NB4	blood:	n/a
14	chr8:124665016-124665066	LNCaP	prostate:	n/a
15	chr8:124665016-124665066	NH-A	brain:	n/a
16	chr8:124665293-124665343	Hela-S3	cervix:	n/a
17	chr8:124665293-124665343	HRCEpiC	kidney:	n/a
18	chr8:124665021-124665071	PFSK-1	brain:	n/a
19	chr8:124665021-124665071	SK-N-MC	brain:	n/a
20	chr8:124665021-124665071	HNPCEpiC	eye:	n/a
21	chr8:124665293-124665343	ECC-1	luminal epithelium:	n/a
22	chr8:124665293-124665343	GM06990	blood:	n/a
23	chr8:124665293-124665343	MCF10A-Er-Src	breast:	n/a
24	chr8:124665293-124665343	Hepatocyte	liver:	n/a
25	chr8:124665016-124665066	AG09309	skin:	n/a
26	chr8:124665016-124665066	CMK	blood:	n/a
27	chr8:124665021-124665071	AG09309	skin:	n/a
28	chr8:124665293-124665343	ProgFib	skin:	n/a
29	chr8:124665016-124665066	GM12892	blood:	n/a
30	chr8:124665021-124665071	AG04449	skin:	fetal
31	chr8:124665016-124665066	HCPEpiC	choroid plexus:	n/a
32	chr8:124665021-124665071	AG09319	gingival:	n/a
33	chr8:124665016-124665066	AG04449	skin:	fetal
34	chr8:124665021-124665071	RPTEC	kidney:	n/a
35	chr8:124665016-124665066	BJ	skin:	n/a
36	chr8:124665293-124665343	LNCaP	prostate:	n/a
37	chr8:124665293-124665343	HEEpiC	esophagus:	n/a
38	chr8:124665293-124665343	H1-hESC	embryonic stem cell:	embryo
39	chr8:124665293-124665343	GM19239	blood:	n/a
40	chr8:124665021-124665071	SAEC	small airway:	n/a
41	chr8:124665021-124665071	HL-60	blood:	n/a
42	chr8:124665016-124665066	HNPCEpiC	eye:	n/a
43	chr8:124665293-124665343	AG04450	lung:	fetal
44	chr8:124665293-124665343	T-47D	breast:	n/a
45	chr8:124665021-124665071	GM12878	blood:	n/a
46	chr8:124665293-124665343	HepG2	liver:	n/a
47	chr8:124665021-124665071	HAEpiC	amniotic membrane:	n/a
48	chr8:124665021-124665071	LNCaP	prostate:	n/a
49	chr8:124665293-124665343	AoSMC	blood vessel:	n/a
50	chr8:124665021-124665071	AG10803	skin:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:124662099..124664193-chr8:124664462..124666029,2	MCF-7	breast:
2	chr8:124655670..124657756-chr8:124660016..124662293,2	K562	blood:
3	chr8:124653035..124654923-chr8:124661285..124663313,2	MCF-7	breast:
4	chr8:124647506..124650348-chr8:124660565..124662892,2	MCF-7	breast:
5	chr8:124658511..124660585-chr8:124661818..124664986,4	MCF-7	breast:

No data

Variant related genes	Relation type
KLHL38	TF binding region
KLHL38	CpG island
ENSG00000175946	chromatin interactions

Extended variants
information (count: 279 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:279 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571592873	chr8:124661507-124661508	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
2	rs534239463	chr8:124661514-124661515	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
3	rs547559877	chr8:124661524-124661525	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
4	rs180831883	chr8:124661578-124661579	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
5	rs138470934	chr8:124661588-124661589	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
6	rs184676156	chr8:124661607-124661608	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
7	rs118094329	chr8:124661660-124661661	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
8	rs58763139	chr8:124661661-124661662	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs559027577	chr8:124661673-124661674	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
10	rs143577866	chr8:124661689-124661690	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
11	rs7387179	chr8:124661695-124661696	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs560244743	chr8:124661723-124661724	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
13	rs573746763	chr8:124661774-124661775	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
14	rs542854810	chr8:124661803-124661804	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
15	rs552411408	chr8:124661831-124661832	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
16	rs570924504	chr8:124661839-124661840	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
17	rs531340166	chr8:124661858-124661859	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
18	rs7386679	chr8:124661905-124661906	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs10505438	chr8:124661919-124661920	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs16898680	chr8:124661934-124661935	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs190211503	chr8:124661954-124661955	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
22	rs536140462	chr8:124661968-124661969	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
23	rs4871404	chr8:124661974-124661975	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs374595759	chr8:124661983-124661984	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
25	rs148627369	chr8:124661990-124661991	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
26	rs182437218	chr8:124661995-124661996	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
27	rs66970129	chr8:124662007-124662008	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs7388119	chr8:124662043-124662044	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs10505439	chr8:124662104-124662105	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs576508375	chr8:124662204-124662205	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs141158969	chr8:124662218-124662219	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13261337	chr8:124662232-124662233	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs13261088	chr8:124662233-124662234	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553781204	chr8:124662244-124662245	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs573907757	chr8:124662254-124662255	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs542443621	chr8:124662257-124662258	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544009062	chr8:124662266-124662267	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150711759	chr8:124662272-124662273	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs185719943	chr8:124662286-124662287	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs564501637	chr8:124662310-124662311	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs13261403	chr8:124662312-124662313	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527280268	chr8:124662340-124662341	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs370966114	chr8:124662341-124662342	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561398722	chr8:124662388-124662389	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs80042966	chr8:124662411-124662412	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs373210004	chr8:124662419-124662420	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs546354989	chr8:124662420-124662421	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs570284107	chr8:124662424-124662425	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs13261937	chr8:124662431-124662432	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs532602878	chr8:124662440-124662441	Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	20932292	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	22056952	CNVD
Langer-Giedion syndrome	16773131	CNVD
Lung cancer	16740712	CNVD
Mental retardation	16773131	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Langer-Giedion syndrome	22470819	CNVD
Cornelia de Lange syndrome	24599119	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Multiple myeloma	17550852	CNVD
Glioblastoma multiforme	18628472	CNVD
Malignant melanoma	17260012	CNVD
Intracranial aneurysm	16715129	CNVD
Breast cancer	16397240	CNVD
Multiple myeloma	16461302	CNVD
Multiple myeloma	16616336	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Breast cancer	21364760	CNVD
Burkitt''s lymphoma	20823134	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Oral squamous cell carcinoma	21853135	CNVD
Breast cancer	21611746	CNVD
Ductal carcinoma	22052326	CNVD
Prostate cancer	22341455	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:124656800-124666000	Weak transcription	HSMM	muscle
2	chr8:124656800-124666800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr8:124657000-124664200	Weak transcription	Placenta	Placenta
4	chr8:124657000-124665600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr8:124658800-124661600	Weak transcription	Right Ventricle	heart
6	chr8:124659000-124661800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr8:124659400-124667000	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr8:124659800-124664200	Weak transcription	Fetal Stomach	stomach
9	chr8:124660000-124662400	Weak transcription	Colon Smooth Muscle	Colon
10	chr8:124660200-124665200	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
11	chr8:124660400-124661800	Enhancers	Fetal Intestine Small	intestine
12	chr8:124660400-124662800	Enhancers	Aorta	Aorta
13	chr8:124660600-124661800	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr8:124660800-124661800	Enhancers	Ovary	ovary
15	chr8:124660800-124662200	Flanking Active TSS	Fetal Heart	heart
16	chr8:124660800-124665400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr8:124661000-124662200	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
18	chr8:124661000-124663600	Active TSS	Left Ventricle	heart
19	chr8:124661000-124666000	Active TSS	Right Atrium	heart
20	chr8:124661200-124661600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:124661200-124661600	Enhancers	A549	lung
22	chr8:124661200-124661800	Active TSS	Stomach Smooth Muscle	stomach
23	chr8:124661200-124662600	Weak transcription	Fetal Intestine Large	intestine
24	chr8:124661200-124663400	Weak transcription	Rectal Smooth Muscle	rectum
25	chr8:124661200-124664200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr8:124661200-124665600	Weak transcription	Osteobl	bone
27	chr8:124661200-124665800	Weak transcription	HSMMtube	muscle
28	chr8:124661200-124665800	Weak transcription	NH-A	brain
29	chr8:124661200-124666000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr8:124661200-124666400	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr8:124661200-124670000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr8:124661400-124661800	Active TSS	Psoas Muscle	Psoas
33	chr8:124661400-124663800	Active TSS	Fetal Muscle Leg	muscle
34	chr8:124661400-124666200	Active TSS	Fetal Muscle Trunk	muscle
35	chr8:124661600-124661800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:124661600-124664400	Active TSS	Right Ventricle	heart
37	chr8:124661800-124662200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr8:124661800-124662200	Flanking Active TSS	Psoas Muscle	Psoas
39	chr8:124661800-124662200	Flanking Active TSS	Stomach Smooth Muscle	stomach
40	chr8:124661800-124664200	Weak transcription	Ovary	ovary
41	chr8:124661800-124664600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr8:124661800-124665000	Weak transcription	Fetal Intestine Small	intestine
43	chr8:124662200-124663200	Active TSS	Fetal Heart	heart
44	chr8:124662200-124663200	Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr8:124662200-124663400	Active TSS	Stomach Smooth Muscle	stomach
46	chr8:124662200-124663800	Active TSS	Psoas Muscle	Psoas
47	chr8:124662200-124664000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr8:124662400-124663800	Enhancers	Colon Smooth Muscle	Colon
49	chr8:124662600-124663000	Enhancers	Fetal Intestine Large	intestine
50	chr8:124662800-124664200	Weak transcription	Aorta	Aorta

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