Variant report

Variant	esv3347263
Chromosome Location	chr21:45204424-45209222
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:653)
CpG islands
(count:549)
Chromatin interactive
region (count:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:653 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr21:45209084-45209502	HepG2	liver:	n/a	n/a
2	ARID3A	chr21:45208981-45209511	K562	blood:	n/a	n/a
3	ATF1	chr21:45209166-45209630	K562	blood:	n/a	n/a
4	ATF2	chr21:45208969-45209208	GM12878	blood:	n/a	n/a
5	ATF2	chr21:45209020-45209650	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr21:45208890-45209674	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr21:45209184-45209791	GM12878	blood:	n/a	n/a
8	ATF3	chr21:45208971-45209664	HepG2	liver:	n/a	chr21:45209303-45209312
9	ATF3	chr21:45208985-45209985	K562	blood:	n/a	chr21:45209303-45209312
10	ATF3	chr21:45209205-45209581	HepG2	liver:	n/a	chr21:45209303-45209312
11	ATF3	chr21:45209097-45209654	K562	blood:	n/a	chr21:45209303-45209312
12	ATF3	chr21:45209150-45209557	GM12878	blood:	n/a	chr21:45209303-45209312
13	ATF3	chr21:45208873-45209622	K562	blood:	n/a	chr21:45209303-45209312
14	ATF3	chr21:45209138-45209618	H1-hESC	embryonic stem cell:	n/a	chr21:45209303-45209312
15	ATF3	chr21:45208964-45209621	GM12878	blood:	n/a	chr21:45209303-45209312
16	ATF3	chr21:45209068-45209641	H1-hESC	embryonic stem cell:	n/a	chr21:45209303-45209312
17	BACH1	chr21:45209000-45209577	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr21:45206784-45207412	GM12878	blood:	n/a	n/a
19	BCL3	chr21:45208383-45208673	GM12878	blood:	n/a	n/a
20	BCL3	chr21:45206212-45206642	GM12878	blood:	n/a	n/a
21	BCL3	chr21:45206201-45207351	GM12878	blood:	n/a	n/a
22	BCLAF1	chr21:45209065-45209651	GM12878	blood:	n/a	chr21:45209229-45209242
23	BHLHE40	chr21:45209199-45209683	K562	blood:	n/a	n/a
24	BHLHE40	chr21:45209073-45209753	GM12878	blood:	n/a	chr21:45209705-45209721 chr21:45209699-45209715
25	BHLHE40	chr21:45209192-45209649	HepG2	liver:	n/a	n/a
26	BRCA1	chr21:45209054-45209590	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chr21:45209219-45209598	H1-hESC	embryonic stem cell:	n/a	n/a
28	CBX3	chr21:45209176-45209499	K562	blood:	n/a	n/a
29	CBX3	chr21:45206320-45207372	K562	blood:	n/a	n/a
30	CBX3	chr21:45206508-45207439	K562	blood:	n/a	n/a
31	CBX3	chr21:45208873-45209671	K562	blood:	n/a	n/a
32	CCNT2	chr21:45209025-45209844	K562	blood:	n/a	n/a
33	CEBPB	chr21:45205087-45205314	HepG2	liver:	n/a	chr21:45205227-45205238
34	CEBPB	chr21:45209222-45209515	K562	blood:	n/a	n/a
35	CEBPB	chr21:45205092-45205353	Hela-S3	cervix:	n/a	chr21:45205227-45205238
36	CEBPB	chr21:45205066-45205372	IMR90	lung:	n/a	chr21:45205227-45205238
37	CEBPB	chr21:45205080-45205257	HepG2	liver:	n/a	chr21:45205227-45205238
38	CEBPB	chr21:45209191-45209602	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr21:45205091-45205281	A549	lung:	n/a	chr21:45205227-45205238
40	CEBPB	chr21:45206451-45206627	A549	lung:	n/a	n/a
41	CEBPB	chr21:45205128-45205323	K562	blood:	n/a	chr21:45205227-45205238
42	CEBPB	chr21:45205125-45205297	H1-hESC	embryonic stem cell:	n/a	chr21:45205227-45205238
43	CEBPB	chr21:45205067-45205307	K562	blood:	n/a	chr21:45205227-45205238
44	CEBPD	chr21:45209052-45209628	K562	blood:	n/a	n/a
45	CEBPD	chr21:45208932-45209546	HepG2	liver:	n/a	n/a
46	CHD2	chr21:45209148-45209676	GM12878	blood:	n/a	n/a
47	CHD2	chr21:45209157-45209592	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr21:45209083-45209594	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr21:45206845-45206961	HepG2	liver:	n/a	n/a
50	CHD2	chr21:45209186-45209590	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr21:45206724-45206774	CMK	blood:	n/a
2	chr21:45208971-45209021	MCF-7	breast:	n/a
3	chr21:45206377-45206427	HPAEpiC	pulmonary alveolar:	n/a
4	chr21:45208971-45209021	GM12891	blood:	n/a
5	chr21:45209045-45209095	GM12878	blood:	n/a
6	chr21:45206377-45206427	SK-N-SH	brain:	n/a
7	chr21:45206377-45206427	HL-60	blood:	n/a
8	chr21:45208971-45209021	AG04450	lung:	fetal
9	chr21:45208169-45208219	NHBE	bronchial:	n/a
10	chr21:45209045-45209095	H1-hESC	embryonic stem cell:	embryo
11	chr21:45206948-45206998	U87	brain:	n/a
12	chr21:45208971-45209021	HCM	heart:	n/a
13	chr21:45206948-45206998	Caco-2	colon:	n/a
14	chr21:45206948-45206998	PFSK-1	brain:	n/a
15	chr21:45209045-45209095	HRCEpiC	kidney:	n/a
16	chr21:45209138-45209188	PANC-1	pancreas:	n/a
17	chr21:45206948-45206998	HNPCEpiC	eye:	n/a
18	chr21:45206377-45206427	RPTEC	kidney:	n/a
19	chr21:45208169-45208219	NT2-D1	testis:	n/a
20	chr21:45206724-45206774	AG10803	skin:	n/a
21	chr21:45206768-45206818	A549	lung:	n/a
22	chr21:45209138-45209188	ProgFib	skin:	n/a
23	chr21:45206768-45206818	AG09309	skin:	n/a
24	chr21:45205511-45205561	Caco-2	colon:	n/a
25	chr21:45206948-45206998	AG04450	lung:	fetal
26	chr21:45206377-45206427	BE2_C	brain:	n/a
27	chr21:45205511-45205561	NHDF-neo	bronchial:	n/a
28	chr21:45208971-45209021	HNPCEpiC	eye:	n/a
29	chr21:45206724-45206774	MCF-7	breast:	n/a
30	chr21:45208169-45208219	NB4	blood:	n/a
31	chr21:45206768-45206818	GM12892	blood:	n/a
32	chr21:45205511-45205561	AG04449	skin:	fetal
33	chr21:45206377-45206427	AoSMC	blood vessel:	n/a
34	chr21:45209138-45209188	IMR90	lung:	fetal
35	chr21:45208971-45209021	HCT-116	colon:	n/a
36	chr21:45205511-45205561	Hela-S3	cervix:	n/a
37	chr21:45206948-45206998	ProgFib	skin:	n/a
38	chr21:45209138-45209188	RPTEC	kidney:	n/a
39	chr21:45209045-45209095	HRE	kidney:	n/a
40	chr21:45206948-45206998	SKMC	muscle:	n/a
41	chr21:45206377-45206427	HCM	heart:	n/a
42	chr21:45206724-45206774	U87	brain:	n/a
43	chr21:45206377-45206427	K562	blood:	n/a
44	chr21:45206377-45206427	NH-A	brain:	n/a
45	chr21:45206724-45206774	HMEC	breast:	n/a
46	chr21:45206768-45206818	HEEpiC	esophagus:	n/a
47	chr21:45206768-45206818	Hepatocyte	liver:	n/a
48	chr21:45208971-45209021	HCF	heart:	n/a
49	chr21:45209045-45209095	HCPEpiC	choroid plexus:	n/a
50	chr21:45206768-45206818	H1-hESC	embryonic stem cell:	embryo

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:45138604..45140519-chr21:45206523..45208517,2	K562	blood:
2	chr21:45138000..45143848-chr21:45206375..45212489,9	MCF-7	breast:
3	chr21:45130981..45133882-chr21:45206562..45209340,2	K562	blood:
4	chr21:45208647..45209350-chr3:12598128..12598853,2	MCF-7	breast:
5	chr21:45207900..45209521-chr21:45431429..45433903,2	MCF-7	breast:
6	chr21:45202942..45205405-chr21:45231641..45234246,2	K562	blood:
7	chr21:45195743..45196721-chr21:45208905..45209461,2	MCF-7	breast:
8	chr21:45205883..45207499-chr21:45284527..45286198,2	K562	blood:
9	chr21:45201612..45205256-chr21:45206995..45210818,5	MCF-7	breast:
10	chr21:45158615..45161441-chr21:45207897..45210708,2	K562	blood:
11	chr21:45207339..45211369-chr21:45429720..45433341,4	K562	blood:
12	chr21:45201612..45205256-chr21:45206995..45210818,5	MCF-7	breast:
13	chr21:45136894..45141532-chr21:45205840..45211872,8	MCF-7	breast:
14	chr21:44912384..44914729-chr21:45206399..45208292,2	MCF-7	breast:
15	chr21:45159250..45162021-chr21:45208113..45211544,3	MCF-7	breast:
16	chr21:45146427..45148749-chr21:45209148..45210811,2	K562	blood:
17	chr21:45193334..45196312-chr21:45207752..45211007,4	MCF-7	breast:
18	chr21:45137987..45140487-chr21:45203011..45205092,2	MCF-7	breast:
19	chr21:45205839..45207709-chr21:45212746..45214269,2	MCF-7	breast:
20	chr21:45076259..45080839-chr21:45207005..45211007,4	MCF-7	breast:
21	chr21:45141091..45143140-chr21:45208651..45211403,2	K562	blood:
22	chr21:45094660..45096892-chr21:45205328..45207677,2	K562	blood:
23	chr21:45137818..45140003-chr21:45203193..45206187,2	MCF-7	breast:
24	chr21:45195028..45197771-chr21:45204736..45207262,2	MCF-7	breast:
25	chr21:45188049..45190841-chr21:45206908..45209310,2	MCF-7	breast:

No data

Variant related genes	Relation type
RRP1	TF binding region
RRP1	CpG island
ENSG00000234030	chromatin interactions
ENSG00000160214	chromatin interactions
ENSG00000160207	chromatin interactions
ENSG00000160209	chromatin interactions
ENSG00000160213	chromatin interactions
ENSG00000160218	chromatin interactions
ENSG00000160208	chromatin interactions
ENSG00000075975	chromatin interactions
ENSG00000160216	chromatin interactions
ENSG00000215458	chromatin interactions

Extended variants
information (count: 229 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:229 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7276461	chr21:45204536-45204537	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550731904	chr21:45204566-45204567	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs35205717	chr21:45204570-45204571	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs144733395	chr21:45204578-45204579	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs148131944	chr21:45204630-45204631	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs572701542	chr21:45204648-45204649	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs534114420	chr21:45204681-45204682	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs558396020	chr21:45204689-45204690	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs576660735	chr21:45204705-45204706	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs560148512	chr21:45204727-45204728	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs562688203	chr21:45204768-45204769	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs28648008	chr21:45204804-45204805	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs541919962	chr21:45204833-45204834	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs560542594	chr21:45204834-45204835	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs374163592	chr21:45204842-45204843	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs546493891	chr21:45204846-45204847	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs28544397	chr21:45204886-45204887	Weak transcription	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs188679318	chr21:45204893-45204894	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs550385374	chr21:45204911-45204912	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs568625905	chr21:45204919-45204920	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs72216816	chr21:45204964-45204965	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs199638645	chr21:45204965-45204966	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs200652006	chr21:45204967-45204968	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs367604871	chr21:45204968-45204969	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs202126955	chr21:45204969-45204970	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs529798384	chr21:45204971-45204972	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs547946531	chr21:45204973-45204974	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs374897097	chr21:45204975-45204976	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs61662383	chr21:45204984-45204985	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs148288476	chr21:45204987-45204988	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs56939645	chr21:45204988-45204989	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs564293765	chr21:45204992-45204993	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs71197862	chr21:45204993-45204994	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs199748095	chr21:45205000-45205001	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs376461273	chr21:45205001-45205002	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs111847023	chr21:45205010-45205011	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs547343329	chr21:45205014-45205015	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs566477222	chr21:45205016-45205017	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs376069245	chr21:45205024-45205025	Weak transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs34726130	chr21:45205040-45205041	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs58119154	chr21:45205041-45205042	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs35834146	chr21:45205049-45205050	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs533537528	chr21:45205055-45205056	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs59035977	chr21:45205061-45205062	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs558452026	chr21:45205077-45205078	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs531362788	chr21:45205113-45205114	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs61160035	chr21:45205209-45205210	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs369013080	chr21:45205210-45205211	Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs190771486	chr21:45205284-45205285	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs9808695	chr21:45205330-45205331	Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:100)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Wilms tumour	21544195	CNVD
Ewing''s sarcoma	17952124	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute myeloid leukemia	16864856	CNVD
Mental retardation	21031080	CNVD
Polymicrogyria	21031080	CNVD
periventricular nodular heterotopia	21031080	CNVD
Myelodysplastic syndrome	21606161	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Autism	18414403	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21858162	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17899364	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	20473283	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Ewing''s sarcoma	21437220	CNVD
Lung adenocarcinoma	17086460	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	21829676	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute myeloid leukemia	21358987	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	23341502	CNVD
Ovarian cancer	21720365	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Neuroblastoma	20406844	CNVD
Acute myeloid leukemia	21251322	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Cholangiocarcinoma	16830362	CNVD
Down syndrome	17334655	CNVD
Neuroticism	17667963	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Autoimmune polyendocrine syndrome	18200029	CNVD
Prostate cancer	19363497	CNVD
Lung cancer	17086460	CNVD
Olfactory neuroblastoma	18408657	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45196800-45206400	Weak transcription	Gastric	stomach
2	chr21:45196800-45206400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr21:45196800-45208800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr21:45196800-45209000	Weak transcription	Aorta	Aorta
5	chr21:45198800-45206400	Weak transcription	Spleen	Spleen
6	chr21:45198800-45206600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr21:45199000-45206400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr21:45199000-45208600	Weak transcription	Stomach Mucosa	stomach
9	chr21:45199000-45208800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr21:45199200-45208400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr21:45199200-45208600	Weak transcription	Primary T cells from cord blood	blood
12	chr21:45199400-45208600	Weak transcription	Primary B cells from cord blood	blood
13	chr21:45200000-45206400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr21:45200600-45204600	Enhancers	NHEK	skin
15	chr21:45200800-45204800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr21:45201000-45206600	Weak transcription	Colonic Mucosa	Colon
17	chr21:45202600-45208600	Weak transcription	Primary T helper cells PMA-I stimulated	--
18	chr21:45203000-45204600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr21:45203200-45208400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr21:45203200-45208800	Weak transcription	HMEC	breast
21	chr21:45203400-45206400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr21:45203400-45208400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
23	chr21:45203400-45208400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr21:45203400-45208400	Weak transcription	GM12878-XiMat	blood
25	chr21:45203600-45206600	Weak transcription	Lung	lung
26	chr21:45203600-45208400	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr21:45203600-45208400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr21:45203600-45208600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr21:45203600-45208600	Weak transcription	A549	lung
30	chr21:45203800-45204600	Enhancers	HepG2	liver
31	chr21:45203800-45206200	Weak transcription	Pancreas	Pancrea
32	chr21:45203800-45206400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr21:45203800-45206400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr21:45203800-45206400	Weak transcription	Hela-S3	cervix
35	chr21:45203800-45208600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr21:45203800-45208600	Weak transcription	Primary hematopoietic stem cells	blood
37	chr21:45203800-45208600	Weak transcription	Adipose Nuclei	Adipose
38	chr21:45203800-45208600	Weak transcription	Monocytes-CD14+_RO01746	blood
39	chr21:45204200-45204800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr21:45204200-45204800	Enhancers	K562	blood
41	chr21:45204400-45204600	Enhancers	Esophagus	oesophagus
42	chr21:45204600-45206400	Weak transcription	Esophagus	oesophagus
43	chr21:45204600-45208600	Weak transcription	HepG2	liver
44	chr21:45204600-45208600	Weak transcription	NHEK	skin
45	chr21:45204600-45209000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr21:45204800-45206000	Weak transcription	K562	blood
47	chr21:45204800-45208400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr21:45204800-45208600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr21:45205000-45208400	Weak transcription	Dnd41	blood
50	chr21:45206200-45206600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin

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