Variant report

Variant	esv3438551
Chromosome Location	chr2:20442021-20443019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:330)
CpG islands
(count:246)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:20442043-20442177	K562	blood:	n/a	n/a
2	BCL3	chr2:20441749-20442258	GM12878	blood:	n/a	chr2:20442206-20442215
3	BCL3	chr2:20442965-20443305	GM12878	blood:	n/a	n/a
4	BCL3	chr2:20442520-20443386	A549	lung:	n/a	n/a
5	BHLHE40	chr2:20442565-20442711	HepG2	liver:	n/a	n/a
6	BHLHE40	chr2:20442118-20442258	K562	blood:	n/a	n/a
7	CCNT2	chr2:20442084-20442284	K562	blood:	n/a	n/a
8	CHD2	chr2:20442060-20442203	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr2:20442083-20442269	A549	lung:	n/a	n/a
10	CTCF	chr2:20442567-20442657	HepG2	liver:	n/a	chr2:20442579-20442588
11	CTCF	chr2:20442140-20442290	HCFaa	heart:	n/a	n/a
12	CTCF	chr2:20442123-20442255	MCF-7	breast:	n/a	n/a
13	CTCF	chr2:20442450-20442676	H1-hESC	embryonic stem cell:	n/a	chr2:20442579-20442588
14	CTCF	chr2:20442083-20442287	HepG2	liver:	n/a	n/a
15	CTCF	chr2:20442060-20442210	SAEC	small airway:	n/a	n/a
16	CTCF	chr2:20441980-20442130	GM12865	blood:	n/a	n/a
17	CTCF	chr2:20442540-20442690	GM12872	blood:	n/a	chr2:20442579-20442588
18	CTCF	chr2:20442160-20442310	GM12871	blood:	n/a	n/a
19	CTCF	chr2:20442040-20442290	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr2:20442040-20442190	GM06990	blood:	n/a	n/a
21	CTCF	chr2:20441880-20442030	HPF	lung:	n/a	n/a
22	CTCF	chr2:20442120-20442270	NHLF	lung:	n/a	n/a
23	CTCF	chr2:20442520-20442670	A549	lung:	n/a	chr2:20442579-20442588
24	CTCF	chr2:20442120-20442270	HPF	lung:	n/a	n/a
25	CTCF	chr2:20442151-20442189	Medullo	brain:	n/a	n/a
26	CTCF	chr2:20442100-20442250	HPF	lung:	n/a	n/a
27	CTCF	chr2:20442480-20442630	GM12868	blood:	n/a	chr2:20442579-20442588
28	CTCF	chr2:20442070-20442283	MCF-7	breast:	n/a	n/a
29	CTCF	chr2:20442180-20442330	GM12878	blood:	n/a	n/a
30	CTCF	chr2:20442120-20442270	HEK293	kidney:	n/a	n/a
31	CTCF	chr2:20442046-20442300	K562	blood:	n/a	n/a
32	CTCF	chr2:20442420-20442570	HMEC	breast:	n/a	n/a
33	CTCF	chr2:20442560-20442830	GM06990	blood:	n/a	chr2:20442579-20442588
34	CTCF	chr2:20442140-20442290	GM12868	blood:	n/a	n/a
35	CTCF	chr2:20442500-20442650	GM12873	blood:	n/a	chr2:20442579-20442588
36	CTCF	chr2:20441940-20442230	WI-38	lung:	n/a	n/a
37	CTCF	chr2:20442120-20442270	GM12874	blood:	n/a	n/a
38	CTCF	chr2:20442120-20442270	AG10803	skin:	n/a	n/a
39	CTCF	chr2:20442083-20442266	GM19239	blood:	n/a	n/a
40	CTCF	chr2:20442080-20442230	GM12875	blood:	n/a	n/a
41	CTCF	chr2:20442180-20442330	BE2_C	brain:	n/a	n/a
42	CTCF	chr2:20442140-20442290	Caco-2	colon:	n/a	n/a
43	CTCF	chr2:20442120-20442270	HFF-Myc	foreskin:	n/a	n/a
44	CTCF	chr2:20442065-20442290	NHEK	skin:	n/a	n/a
45	CTCF	chr2:20442177-20442231	MCF-7	breast:	n/a	n/a
46	CTCF	chr2:20442480-20442630	GM12864	blood:	n/a	chr2:20442579-20442588
47	CTCF	chr2:20442060-20442210	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr2:20442560-20442710	K562	blood:	n/a	chr2:20442579-20442588
49	CTCF	chr2:20442040-20442190	HPAF	blood vessel:	n/a	n/a
50	CTCF	chr2:20442039-20442297	GM19240	blood:	n/a	n/a

(count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:20442131-20442181	SKMC	muscle:	n/a
2	chr2:20442131-20442181	HUVEC	blood vessel:	n/a
3	chr2:20442131-20442181	SKMC	muscle:	n/a
4	chr2:20442131-20442181	HUVEC	blood vessel:	n/a
5	chr2:20441979-20442029	MCF-7	breast:	n/a
6	chr2:20441979-20442029	BE2_C	brain:	n/a
7	chr2:20442210-20442260	IMR90	lung:	fetal
8	chr2:20442088-20442138	HUVEC	blood vessel:	n/a
9	chr2:20442088-20442138	HCT-116	colon:	n/a
10	chr2:20442131-20442181	T-47D	breast:	n/a
11	chr2:20442131-20442181	HIPEpiC	eye:	n/a
12	chr2:20442088-20442138	K562	blood:	n/a
13	chr2:20441979-20442029	SK-N-SH_RA	brain:	n/a
14	chr2:20442210-20442260	NT2-D1	testis:	n/a
15	chr2:20441979-20442029	Hepatocyte	liver:	n/a
16	chr2:20442131-20442181	NB4	blood:	n/a
17	chr2:20441979-20442029	MCF10A-Er-Src	breast:	n/a
18	chr2:20441979-20442029	HNPCEpiC	eye:	n/a
19	chr2:20442088-20442138	HL-60	blood:	n/a
20	chr2:20441979-20442029	A549	lung:	n/a
21	chr2:20442131-20442181	H1-hESC	embryonic stem cell:	embryo
22	chr2:20441979-20442029	HAEpiC	amniotic membrane:	n/a
23	chr2:20442210-20442260	HEK293	kidney:	embryo
24	chr2:20442131-20442181	NHBE	bronchial:	n/a
25	chr2:20441979-20442029	ECC-1	luminal epithelium:	n/a
26	chr2:20442131-20442181	PFSK-1	brain:	n/a
27	chr2:20442210-20442260	HepG2	liver:	n/a
28	chr2:20442131-20442181	PrEC	prostate:	n/a
29	chr2:20442088-20442138	HRE	kidney:	n/a
30	chr2:20442131-20442181	SAEC	small airway:	n/a
31	chr2:20442210-20442260	Caco-2	colon:	n/a
32	chr2:20442210-20442260	RPTEC	kidney:	n/a
33	chr2:20441979-20442029	HRE	kidney:	n/a
34	chr2:20442131-20442181	Hela-S3	cervix:	n/a
35	chr2:20442210-20442260	Jurkat	blood:	n/a
36	chr2:20441979-20442029	AG09319	gingival:	n/a
37	chr2:20441979-20442029	HL-60	blood:	n/a
38	chr2:20441979-20442029	ProgFib	skin:	n/a
39	chr2:20442088-20442138	AG04449	skin:	fetal
40	chr2:20442088-20442138	HIPEpiC	eye:	n/a
41	chr2:20442210-20442260	GM12878	blood:	n/a
42	chr2:20442088-20442138	HMEC	breast:	n/a
43	chr2:20442210-20442260	GM12892	blood:	n/a
44	chr2:20442088-20442138	HCM	heart:	n/a
45	chr2:20442210-20442260	T-47D	breast:	n/a
46	chr2:20442210-20442260	BJ	skin:	n/a
47	chr2:20442088-20442138	SK-N-MC	brain:	n/a
48	chr2:20442131-20442181	ovcar-3	ovarian:	n/a
49	chr2:20442210-20442260	HL-60	blood:	n/a
50	chr2:20441979-20442029	HIPEpiC	eye:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:20438741..20440683-chr2:20441500..20444456,2	MCF-7	breast:
2	chr2:20441679..20444514-chr2:20449489..20452544,3	K562	blood:
3	chr2:20335122..20335719-chr2:20442089..20442630,2	K562	blood:
4	chr2:20437602..20439619-chr2:20440851..20444211,3	MCF-7	breast:
5	chr2:20441705..20442588-chr2:20850479..20850992,2	K562	blood:
6	chr2:20422151..20423763-chr2:20440457..20442911,2	MCF-7	breast:
7	chr2:20432388..20434846-chr2:20442190..20444125,2	MCF-7	breast:
8	chr2:20422608..20425941-chr2:20442995..20447318,5	MCF-7	breast:
9	chr2:20425935..20426603-chr2:20441699..20442616,3	MCF-7	breast:
10	chr2:20442462..20444292-chr2:20444678..20446517,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000235411	TF binding region
ENSG00000235411	CpG island
ENSG00000238735	chromatin interactions
ENSG00000115884	chromatin interactions
ENSG00000118960	chromatin interactions

Extended variants
information (count: 39 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:39 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183392933	chr2:20442024-20442025	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs369927023	chr2:20442060-20442061	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs575527261	chr2:20442078-20442079	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs570946882	chr2:20442124-20442125	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs201182131	chr2:20442129-20442130	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs529613388	chr2:20442150-20442151	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs544736067	chr2:20442151-20442152	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs372485930	chr2:20442183-20442184	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs575094685	chr2:20442191-20442192	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs540783397	chr2:20442215-20442216	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs536700357	chr2:20442220-20442221	Weak transcription Enhancers Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs62123434	chr2:20442270-20442271	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs187709655	chr2:20442309-20442310	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs397939291	chr2:20442316-20442317	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs552580469	chr2:20442354-20442355	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs201130842	chr2:20442378-20442379	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs562533210	chr2:20442401-20442402	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs192271679	chr2:20442419-20442420	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs548306710	chr2:20442424-20442425	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs567778609	chr2:20442450-20442451	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs62123435	chr2:20442457-20442458	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs527490242	chr2:20442551-20442552	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs547163436	chr2:20442594-20442595	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs7563245	chr2:20442631-20442632	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs147507164	chr2:20442707-20442708	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs553218549	chr2:20442715-20442716	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs183429622	chr2:20442719-20442720	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569271951	chr2:20442725-20442726	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs72785282	chr2:20442733-20442734	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs188464879	chr2:20442738-20442739	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs371472381	chr2:20442741-20442742	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs140118353	chr2:20442762-20442763	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs540844701	chr2:20442829-20442830	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs554440436	chr2:20442867-20442868	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs7575580	chr2:20442871-20442872	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs7602723	chr2:20442887-20442888	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs192727264	chr2:20442899-20442900	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs531348915	chr2:20442923-20442924	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs56355022	chr2:20442989-20442990	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Medulloblastoma	22160402	CNVD
Schizophrenia	22118685	CNVD
Epilepsy	22118685	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	17908972	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	18765546	CNVD
Neuroblastoma	18281664	CNVD
Neuroblastoma	17289879	CNVD
Neuroblastoma	19738985	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:138 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20426000-20447000	Weak transcription	GM12878-XiMat	blood
2	chr2:20431400-20446800	Weak transcription	Spleen	Spleen
3	chr2:20431800-20444200	Weak transcription	A549	lung
4	chr2:20431800-20446200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr2:20433000-20450200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:20433000-20451200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:20436200-20446600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr2:20436200-20447000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr2:20436600-20452600	Weak transcription	Gastric	stomach
10	chr2:20436800-20445800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr2:20437000-20446400	Weak transcription	Hela-S3	cervix
12	chr2:20437000-20447000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr2:20437000-20453000	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr2:20437800-20448000	Weak transcription	HMEC	breast
15	chr2:20438000-20445600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr2:20439400-20447200	Weak transcription	Primary B cells from cord blood	blood
17	chr2:20439800-20450200	Weak transcription	Brain Substantia Nigra	brain
18	chr2:20440200-20444400	Enhancers	Placenta	Placenta
19	chr2:20440600-20443000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr2:20440600-20446600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:20440600-20447000	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr2:20440600-20451000	Weak transcription	Brain Cingulate Gyrus	brain
23	chr2:20440600-20452600	Weak transcription	Brain Hippocampus Middle	brain
24	chr2:20440800-20445600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr2:20440800-20452200	Weak transcription	Brain Angular Gyrus	brain
26	chr2:20440800-20452600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr2:20441400-20442200	Enhancers	Primary T helper cells PMA-I stimulated	--
28	chr2:20441400-20442800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr2:20441400-20453000	Weak transcription	Pancreatic Islets	Pancreatic Islet
30	chr2:20441600-20442200	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr2:20441600-20442200	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr2:20441600-20442200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr2:20441800-20442200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr2:20441800-20442200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr2:20441800-20442200	Enhancers	Esophagus	oesophagus
36	chr2:20441800-20442200	Flanking Active TSS	Fetal Intestine Large	intestine
37	chr2:20441800-20442200	Flanking Active TSS	Fetal Intestine Small	intestine
38	chr2:20441800-20442200	Enhancers	Right Ventricle	heart
39	chr2:20441800-20442200	Enhancers	Stomach Mucosa	stomach
40	chr2:20441800-20442200	Enhancers	K562	blood
41	chr2:20441800-20442400	Enhancers	HepG2	liver
42	chr2:20441800-20442600	Enhancers	Fetal Thymus	thymus
43	chr2:20441800-20442800	Enhancers	Primary hematopoietic stem cells	blood
44	chr2:20441800-20443200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr2:20441800-20447000	Weak transcription	Adipose Nuclei	Adipose
46	chr2:20441800-20447000	Weak transcription	Duodenum Smooth Muscle	Duodenum
47	chr2:20442000-20442200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
48	chr2:20442000-20442200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
49	chr2:20442000-20442200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr2:20442000-20442200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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