Variant report

Variant	nsv873882
Chromosome Location	chr2:38858669-38921498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1420)
CpG islands
(count:855)
Chromatin interactive
region (count:119)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1420 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:38861740-38862106	K562	blood:	n/a	n/a
2	ARID3A	chr2:38863497-38863532	K562	blood:	n/a	n/a
3	ARID3A	chr2:38917946-38918443	K562	blood:	n/a	n/a
4	ARID3A	chr2:38892880-38893239	K562	blood:	n/a	n/a
5	ARID3A	chr2:38919989-38920328	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:38892806-38893881	HepG2	liver:	n/a	n/a
7	ARID3A	chr2:38881524-38881720	HepG2	liver:	n/a	n/a
8	ARID3A	chr2:38879587-38880043	K562	blood:	n/a	n/a
9	ARID3A	chr2:38912238-38912805	HepG2	liver:	n/a	n/a
10	ARID3A	chr2:38904891-38905252	HepG2	liver:	n/a	n/a
11	ARID3A	chr2:38893914-38894509	K562	blood:	n/a	chr2:38894121-38894137
12	ARID3A	chr2:38895975-38896159	K562	blood:	n/a	n/a
13	ARID3A	chr2:38917822-38918426	HepG2	liver:	n/a	n/a
14	ARID3A	chr2:38870825-38871318	K562	blood:	n/a	n/a
15	ARID3A	chr2:38880715-38881014	K562	blood:	n/a	n/a
16	ATF1	chr2:38879564-38879931	K562	blood:	n/a	n/a
17	ATF1	chr2:38918045-38918315	K562	blood:	n/a	n/a
18	ATF1	chr2:38881066-38882442	K562	blood:	n/a	n/a
19	ATF1	chr2:38870842-38871367	K562	blood:	n/a	n/a
20	ATF1	chr2:38861864-38862095	K562	blood:	n/a	n/a
21	ATF2	chr2:38892778-38893287	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr2:38861670-38862301	GM12878	blood:	n/a	n/a
23	ATF2	chr2:38880502-38881325	GM12878	blood:	n/a	n/a
24	ATF2	chr2:38892876-38893286	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr2:38890859-38891427	GM12878	blood:	n/a	n/a
26	ATF2	chr2:38861690-38862196	GM12878	blood:	n/a	n/a
27	ATF2	chr2:38893966-38894436	GM12878	blood:	n/a	n/a
28	ATF2	chr2:38893915-38894596	GM12878	blood:	n/a	n/a
29	ATF3	chr2:38917860-38918466	A549	lung:	n/a	n/a
30	ATF3	chr2:38870859-38871314	K562	blood:	n/a	n/a
31	ATF3	chr2:38917973-38918312	K562	blood:	n/a	n/a
32	ATF3	chr2:38917844-38918491	A549	lung:	n/a	n/a
33	ATF3	chr2:38892941-38893712	A549	lung:	n/a	n/a
34	ATF3	chr2:38912253-38912923	A549	lung:	n/a	n/a
35	BATF	chr2:38914812-38915129	GM12878	blood:	n/a	n/a
36	BATF	chr2:38880553-38881370	GM12878	blood:	n/a	n/a
37	BATF	chr2:38859186-38859514	GM12878	blood:	n/a	n/a
38	BATF	chr2:38890987-38891390	GM12878	blood:	n/a	n/a
39	BCL11A	chr2:38861720-38862141	GM12878	blood:	n/a	n/a
40	BCL11A	chr2:38880543-38881471	GM12878	blood:	n/a	n/a
41	BCL11A	chr2:38890965-38891338	GM12878	blood:	n/a	n/a
42	BCL3	chr2:38892736-38893577	A549	lung:	n/a	n/a
43	BCL3	chr2:38861808-38862179	GM12878	blood:	n/a	n/a
44	BCL3	chr2:38917723-38918506	A549	lung:	n/a	chr2:38918285-38918292
45	BCL3	chr2:38912120-38913350	A549	lung:	n/a	n/a
46	BCL3	chr2:38912275-38913346	A549	lung:	n/a	n/a
47	BCL3	chr2:38880884-38881268	GM12878	blood:	n/a	n/a
48	BCL3	chr2:38917811-38918387	A549	lung:	n/a	chr2:38918285-38918292
49	BCL3	chr2:38890959-38891353	GM12878	blood:	n/a	n/a
50	BCLAF1	chr2:38890948-38891335	GM12878	blood:	n/a	n/a

(count:855 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:38870290-38870340	GM06990	blood:	n/a
2	chr2:38870290-38870340	GM06990	blood:	n/a
3	chr2:38892365-38892415	NB4	blood:	n/a
4	chr2:38892365-38892415	HCM	heart:	n/a
5	chr2:38870290-38870340	Hepatocyte	liver:	n/a
6	chr2:38894198-38894248	HUVEC	blood vessel:	n/a
7	chr2:38892365-38892415	AoSMC	blood vessel:	n/a
8	chr2:38892846-38892896	SK-N-SH_RA	brain:	n/a
9	chr2:38870535-38870585	Caco-2	colon:	n/a
10	chr2:38892887-38892937	GM06990	blood:	n/a
11	chr2:38919351-38919401	HRE	kidney:	n/a
12	chr2:38893237-38893287	AG09309	skin:	n/a
13	chr2:38870290-38870340	HAEpiC	amniotic membrane:	n/a
14	chr2:38892958-38893008	SK-N-MC	brain:	n/a
15	chr2:38870535-38870585	BE2_C	brain:	n/a
16	chr2:38870290-38870340	RPTEC	kidney:	n/a
17	chr2:38870535-38870585	HL-60	blood:	n/a
18	chr2:38893237-38893287	HRCEpiC	kidney:	n/a
19	chr2:38893519-38893569	ovcar-3	ovarian:	n/a
20	chr2:38893519-38893569	SKMC	muscle:	n/a
21	chr2:38894198-38894248	T-47D	breast:	n/a
22	chr2:38893251-38893301	HEEpiC	esophagus:	n/a
23	chr2:38892901-38892951	NH-A	brain:	n/a
24	chr2:38893251-38893301	AoSMC	blood vessel:	n/a
25	chr2:38894198-38894248	Hela-S3	cervix:	n/a
26	chr2:38892887-38892937	Hepatocyte	liver:	n/a
27	chr2:38892846-38892896	BJ	skin:	n/a
28	chr2:38892309-38892359	MCF-7	breast:	n/a
29	chr2:38893251-38893301	ECC-1	luminal epithelium:	n/a
30	chr2:38893161-38893211	HIPEpiC	eye:	n/a
31	chr2:38893251-38893301	BJ	skin:	n/a
32	chr2:38893161-38893211	SAEC	small airway:	n/a
33	chr2:38893161-38893211	AG09319	gingival:	n/a
34	chr2:38892846-38892896	HCM	heart:	n/a
35	chr2:38894198-38894248	U87	brain:	n/a
36	chr2:38893251-38893301	HRE	kidney:	n/a
37	chr2:38892901-38892951	Jurkat	blood:	n/a
38	chr2:38893237-38893287	A549	lung:	n/a
39	chr2:38893237-38893287	HCF	heart:	n/a
40	chr2:38893251-38893301	CMK	blood:	n/a
41	chr2:38919351-38919401	AG04449	skin:	fetal
42	chr2:38870535-38870585	NT2-D1	testis:	n/a
43	chr2:38893519-38893569	SK-N-MC	brain:	n/a
44	chr2:38893251-38893301	AG09309	skin:	n/a
45	chr2:38893237-38893287	HL-60	blood:	n/a
46	chr2:38892365-38892415	HAEpiC	amniotic membrane:	n/a
47	chr2:38892365-38892415	NHDF-neo	bronchial:	n/a
48	chr2:38892846-38892896	HL-60	blood:	n/a
49	chr2:38892846-38892896	SKMC	muscle:	n/a
50	chr2:38892901-38892951	HAEpiC	amniotic membrane:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:38906476..38910309-chr2:38910692..38914128,4	K562	blood:
2	chr2:38824811..38832919-chr2:38891494..38898299,16	K562	blood:
3	chr2:38827954..38830677-chr2:38913858..38916720,4	K562	blood:
4	chr2:38846799..38849062-chr2:38862889..38864827,2	K562	blood:
5	chr2:38829011..38830871-chr2:38864426..38867339,2	MCF-7	breast:
6	chr2:38895714..38897624-chr2:38914031..38916538,2	K562	blood:
7	chr2:38828302..38829916-chr2:38889127..38891080,2	K562	blood:
8	chr2:38912803..38914727-chr2:38916699..38918326,2	MCF-7	breast:
9	chr2:38826349..38827886-chr2:38868902..38871204,2	K562	blood:
10	chr2:38880141..38882510-chr2:38904571..38906681,2	K562	blood:
11	chr2:38829496..38831232-chr2:38893143..38894875,2	MCF-7	breast:
12	chr2:38909532..38914838-chr2:38917160..38922190,4	K562	blood:
13	chr2:38857535..38860181-chr2:38880883..38883565,2	K562	blood:
14	chr2:38896241..38898904-chr2:38899208..38901062,2	MCF-7	breast:
15	chr2:38862386..38864039-chr2:38870726..38872820,2	K562	blood:
16	chr2:38917783..38919456-chr2:38977277..38979712,2	MCF-7	breast:
17	chr2:38895186..38897690-chr2:38903114..38905637,2	K562	blood:
18	chr2:38887947..38890064-chr2:38891296..38894559,3	K562	blood:
19	chr2:38826787..38832652-chr2:38859055..38867252,11	K562	blood:
20	chr2:38893888..38897011-chr2:38898419..38901251,3	K562	blood:
21	chr2:38914950..38917916-chr2:38919871..38923223,3	K562	blood:
22	chr2:38823862..38826061-chr2:38919360..38922289,2	K562	blood:
23	chr2:38891733..38894492-chr2:38894527..38896151,2	K562	blood:
24	chr2:38917976..38920812-chr2:38977039..38979793,2	K562	blood:
25	chr2:38876173..38878521-chr2:38919650..38921533,2	MCF-7	breast:
26	chr2:38826731..38830931-chr2:38855127..38860520,4	MCF-7	breast:
27	chr2:38872329..38875260-chr2:38918256..38921155,2	K562	blood:
28	chr2:38897993..38900823-chr2:38904497..38907341,3	K562	blood:
29	chr2:38884843..38887789-chr2:38891442..38893148,3	K562	blood:
30	chr2:38823625..38826319-chr2:38903588..38906507,3	K562	blood:
31	chr2:38872329..38875260-chr2:38918256..38921155,2	K562	blood:
32	chr2:38818005..38820191-chr2:38893287..38895221,2	K562	blood:
33	chr2:38908524..38910141-chr2:38911332..38912843,2	MCF-7	breast:
34	chr2:38857535..38860181-chr2:38880883..38883565,2	K562	blood:
35	chr2:38903554..38905525-chr2:38909598..38912564,2	MCF-7	breast:
36	chr2:38892930..38895051-chr2:38905642..38907216,2	K562	blood:
37	chr2:38823851..38826080-chr2:38908814..38911340,2	K562	blood:
38	chr2:38777679..38779633-chr2:38893883..38895640,2	K562	blood:
39	chr2:38893261..38895190-chr2:38902040..38904878,2	K562	blood:
40	chr2:38880141..38882510-chr2:38904571..38906681,2	K562	blood:
41	chr2:38827420..38830831-chr2:38879840..38883102,4	K562	blood:
42	chr2:38866346..38869051-chr2:38869593..38871787,4	K562	blood:
43	chr2:38876173..38878521-chr2:38919650..38921533,2	MCF-7	breast:
44	chr2:38915899..38920812-chr2:38977039..38979793,4	K562	blood:
45	chr2:38827470..38830831-chr2:38880188..38882467,3	K562	blood:
46	chr2:38838640..38841229-chr2:38869315..38872620,3	K562	blood:
47	chr2:38829210..38832278-chr2:38859055..38864456,6	K562	blood:
48	chr2:38885587..38887853-chr2:38899789..38902113,2	K562	blood:
49	chr2:38918111..38919788-chr2:38928353..38930489,2	K562	blood:
50	chr2:38828129..38829795-chr2:38916759..38919645,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HNRPLL-2	chr2:38895830-38895903	ENSG00000232518.1
2	lnc-HNRPLL-2	chr2:38896481-38896680	ENSG00000232518.1
3	lnc-HNRPLL-2	chr2:38896001-38896210	ENSG00000232518.1
4	lnc-HNRPLL-2	chr2:38898496-38898563	ENSG00000232518.1

No data

Variant related genes	Relation type
GALM	TF binding region
ENSG00000232518	TF binding region
GALM	CpG island
ENSG00000232518	CpG island
ENSG00000232518	chromatin interactions
ENSG00000136478	chromatin interactions
ENSG00000143889	chromatin interactions
ENSG00000235586	chromatin interactions
ENSG00000143891	chromatin interactions
ENSG00000115875	chromatin interactions
ENSG00000152147	chromatin interactions

Extended variants
information (count: 3246 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3246 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10204680	chr2:38858669-38858670	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs10204707	chr2:38858759-38858760	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs370056393	chr2:38858776-38858777	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs34145681	chr2:38858831-38858832	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs149131666	chr2:38858853-38858854	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs188124857	chr2:38858854-38858855	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs192873218	chr2:38858888-38858889	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs576333956	chr2:38858956-38858957	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs537571293	chr2:38858957-38858958	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs184550113	chr2:38858991-38858992	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs574186121	chr2:38858995-38858996	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs55820712	chr2:38859000-38859001	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs186767046	chr2:38859057-38859058	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs577959891	chr2:38859123-38859124	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545281547	chr2:38859136-38859137	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs563324798	chr2:38859137-38859138	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs530397248	chr2:38859149-38859150	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs549080309	chr2:38859150-38859151	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs538400022	chr2:38859179-38859180	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs543580367	chr2:38859205-38859206	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs191266858	chr2:38859245-38859246	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs143408624	chr2:38859263-38859264	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs151322613	chr2:38859267-38859268	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs538961626	chr2:38859275-38859276	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs550863972	chr2:38859279-38859280	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs80122974	chr2:38859306-38859307	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs537004466	chr2:38859319-38859320	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs565395175	chr2:38859323-38859324	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs555833516	chr2:38859329-38859330	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs574096659	chr2:38859340-38859341	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs578162204	chr2:38859342-38859343	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs2217537	chr2:38859364-38859365	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs373403987	chr2:38859385-38859386	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs58892329	chr2:38859408-38859409	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs184927392	chr2:38859476-38859477	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs545316697	chr2:38859480-38859481	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs551592381	chr2:38859590-38859591	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs563794606	chr2:38859600-38859601	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs571338366	chr2:38859626-38859627	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs111714671	chr2:38859630-38859631	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs201331354	chr2:38859631-38859632	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs575208035	chr2:38859634-38859635	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs556808950	chr2:38859647-38859648	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs140572841	chr2:38859655-38859656	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs189361726	chr2:38859656-38859657	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs200477205	chr2:38859658-38859659	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs201898255	chr2:38859659-38859660	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs79918284	chr2:38859662-38859663	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs181790152	chr2:38859679-38859680	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs565095477	chr2:38859699-38859700	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	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
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	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
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Non-small cell lung cancer	18927303	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Colorectal cancer	16272173	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1818 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:38835400-38862400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:38854000-38861200	Weak transcription	Primary T cells from cord blood	blood
3	chr2:38857400-38859000	Weak transcription	GM12878-XiMat	blood
4	chr2:38858000-38861000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr2:38859000-38860400	Enhancers	GM12878-XiMat	blood
6	chr2:38860400-38860800	Weak transcription	GM12878-XiMat	blood
7	chr2:38860800-38861200	Enhancers	GM12878-XiMat	blood
8	chr2:38861000-38861400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr2:38861000-38862200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr2:38861000-38862200	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr2:38861000-38862400	Enhancers	Dnd41	blood
12	chr2:38861000-38862600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr2:38861000-38862600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr2:38861000-38862600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr2:38861000-38862800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
16	chr2:38861000-38863600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr2:38861200-38861600	Flanking Active TSS	GM12878-XiMat	blood
18	chr2:38861200-38862000	Enhancers	Primary T cells from cord blood	blood
19	chr2:38861200-38862000	Enhancers	Hela-S3	cervix
20	chr2:38861200-38862000	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr2:38861200-38862600	Enhancers	Primary hematopoietic stem cells	blood
22	chr2:38861200-38862800	Enhancers	Primary monocytes fromperipheralblood	blood
23	chr2:38861400-38862200	Enhancers	HepG2	liver
24	chr2:38861400-38862800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
25	chr2:38861400-38863000	Enhancers	K562	blood
26	chr2:38861600-38862000	Enhancers	Primary T helper naive cells from peripheral blood	blood
27	chr2:38861600-38862000	Active TSS	GM12878-XiMat	blood
28	chr2:38861600-38862200	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr2:38861600-38862200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr2:38861800-38862000	Enhancers	Thymus	Thymus
31	chr2:38861800-38862600	Enhancers	Primary B cells from peripheral blood	blood
32	chr2:38861800-38862600	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr2:38861800-38862600	Enhancers	Fetal Thymus	thymus
34	chr2:38862000-38862400	Flanking Active TSS	GM12878-XiMat	blood
35	chr2:38862000-38862400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
36	chr2:38862000-38862800	Enhancers	Primary B cells from cord blood	blood
37	chr2:38862400-38862600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr2:38862400-38862800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:38862400-38862800	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr2:38862400-38863000	Enhancers	GM12878-XiMat	blood
41	chr2:38862600-38862800	Enhancers	Thymus	Thymus
42	chr2:38862800-38870000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr2:38862800-38870200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr2:38863000-38863200	Weak transcription	K562	blood
45	chr2:38863200-38863400	Enhancers	Stomach Mucosa	stomach
46	chr2:38863200-38863600	Enhancers	K562	blood
47	chr2:38863400-38864000	Weak transcription	Stomach Mucosa	stomach
48	chr2:38863600-38864000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr2:38863600-38869800	Weak transcription	K562	blood
50	chr2:38864000-38864200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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