Variant report

Variant	nsv834473
Chromosome Location	chr2:180864256-181030940
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1800)
CpG islands
(count:1404)
Chromatin interactive
region (count:59)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1800 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:180877312-180877545	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:180871673-180872285	K562	blood:	n/a	n/a
3	ARID3A	chr2:180866653-180866746	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:180942069-180942378	HepG2	liver:	n/a	n/a
5	ARID3A	chr2:180871155-180871309	K562	blood:	n/a	n/a
6	ARID3A	chr2:180942029-180942384	K562	blood:	n/a	n/a
7	ARID3A	chr2:180871585-180872271	HepG2	liver:	n/a	n/a
8	ATF1	chr2:180921964-180922115	K562	blood:	n/a	n/a
9	ATF1	chr2:180975288-180975510	K562	blood:	n/a	n/a
10	ATF1	chr2:180898977-180899263	K562	blood:	n/a	n/a
11	ATF1	chr2:180885680-180885829	K562	blood:	n/a	n/a
12	ATF1	chr2:180871557-180872292	K562	blood:	n/a	n/a
13	ATF2	chr2:180871438-180872353	GM12878	blood:	n/a	n/a
14	ATF2	chr2:180871594-180872244	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr2:180921356-180921970	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr2:180921413-180921941	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr2:180990251-180990564	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr2:180871642-180872143	GM12878	blood:	n/a	n/a
19	ATF3	chr2:180898965-180899192	K562	blood:	n/a	n/a
20	BATF	chr2:180870246-180870466	GM12878	blood:	n/a	n/a
21	BCL11A	chr2:180921557-180921833	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr2:180883149-180883358	GM12878	blood:	n/a	n/a
23	BCL3	chr2:180883821-180884183	GM12878	blood:	n/a	n/a
24	BCL3	chr2:180885255-180885731	GM12878	blood:	n/a	n/a
25	BCL3	chr2:180885395-180885693	GM12878	blood:	n/a	n/a
26	BCL3	chr2:180902985-180903282	GM12878	blood:	n/a	n/a
27	BCL3	chr2:180883366-180884390	GM12878	blood:	n/a	n/a
28	BCLAF1	chr2:180871686-180872197	GM12878	blood:	n/a	n/a
29	BHLHE40	chr2:180870895-180872194	K562	blood:	n/a	n/a
30	BHLHE40	chr2:180869631-180869781	K562	blood:	n/a	n/a
31	BHLHE40	chr2:180898968-180899579	K562	blood:	n/a	n/a
32	BHLHE40	chr2:180903755-180904022	GM12878	blood:	n/a	n/a
33	BRCA1	chr2:180872401-180872488	HepG2	liver:	n/a	n/a
34	BRCA1	chr2:180871679-180871856	GM12878	blood:	n/a	n/a
35	BRCA1	chr2:180871695-180872248	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr2:181012368-181012453	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr2:180882110-180882218	GM12878	blood:	n/a	n/a
38	BRCA1	chr2:180871487-180872178	HepG2	liver:	n/a	n/a
39	CBX3	chr2:180990073-180990924	HCT-116	colon:	n/a	n/a
40	CBX3	chr2:180871375-180872394	K562	blood:	n/a	n/a
41	CCNT2	chr2:180975287-180975516	K562	blood:	n/a	n/a
42	CEBPB	chr2:180877236-180877655	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr2:180987601-180987907	IMR90	lung:	n/a	n/a
44	CEBPB	chr2:180959549-180959712	HepG2	liver:	n/a	chr2:180959632-180959643
45	CEBPB	chr2:180871765-180872223	A549	lung:	n/a	n/a
46	CEBPB	chr2:180914991-180915328	IMR90	lung:	n/a	n/a
47	CEBPB	chr2:180877300-180877674	HepG2	liver:	n/a	n/a
48	CEBPB	chr2:180871757-180872201	HepG2	liver:	n/a	n/a
49	CEBPB	chr2:180976760-180976923	H1-hESC	embryonic stem cell:	n/a	chr2:180976824-180976835 chr2:180976824-180976837
50	CEBPB	chr2:180877392-180877649	A549	lung:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:180871757-180871807	K562	blood:	n/a
2	chr2:180871757-180871807	K562	blood:	n/a
3	chr2:180921730-180921780	ECC-1	luminal epithelium:	n/a
4	chr2:180881175-180881225	MCF10A-Er-Src	breast:	n/a
5	chr2:180871787-180871837	AG09319	gingival:	n/a
6	chr2:180936706-180936756	T-47D	breast:	n/a
7	chr2:180921730-180921780	H1-hESC	embryonic stem cell:	embryo
8	chr2:180881175-180881225	HEEpiC	esophagus:	n/a
9	chr2:180872115-180872165	Jurkat	blood:	n/a
10	chr2:180886672-180886722	Jurkat	blood:	n/a
11	chr2:180989671-180989721	HNPCEpiC	eye:	n/a
12	chr2:180869803-180869853	T-47D	breast:	n/a
13	chr2:180872142-180872192	A549	lung:	n/a
14	chr2:180871811-180871861	HEK293	kidney:	embryo
15	chr2:180875203-180875253	Jurkat	blood:	n/a
16	chr2:180871757-180871807	HUVEC	blood vessel:	n/a
17	chr2:180886778-180886828	IMR90	lung:	fetal
18	chr2:180899188-180899238	HNPCEpiC	eye:	n/a
19	chr2:180886608-180886658	BJ	skin:	n/a
20	chr2:180872053-180872103	Jurkat	blood:	n/a
21	chr2:180921730-180921780	ovcar-3	ovarian:	n/a
22	chr2:180990502-180990552	AG04450	lung:	fetal
23	chr2:180871787-180871837	ProgFib	skin:	n/a
24	chr2:180868811-180868861	AG04449	skin:	fetal
25	chr2:180886778-180886828	Caco-2	colon:	n/a
26	chr2:180869803-180869853	HUVEC	blood vessel:	n/a
27	chr2:180936706-180936756	PFSK-1	brain:	n/a
28	chr2:180869803-180869853	ProgFib	skin:	n/a
29	chr2:180871811-180871861	AG09319	gingival:	n/a
30	chr2:180868811-180868861	HUVEC	blood vessel:	n/a
31	chr2:180871787-180871837	RPTEC	kidney:	n/a
32	chr2:180872142-180872192	AG09309	skin:	n/a
33	chr2:180881175-180881225	Jurkat	blood:	n/a
34	chr2:180869803-180869853	MCF10A-Er-Src	breast:	n/a
35	chr2:180936706-180936756	SK-N-SH	brain:	n/a
36	chr2:180921730-180921780	SKMC	muscle:	n/a
37	chr2:180875203-180875253	ovcar-3	ovarian:	n/a
38	chr2:180869803-180869853	ovcar-3	ovarian:	n/a
39	chr2:180886672-180886722	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:180871811-180871861	RPTEC	kidney:	n/a
41	chr2:180871780-180871830	RPTEC	kidney:	n/a
42	chr2:180886608-180886658	NH-A	brain:	n/a
43	chr2:181010312-181010362	U87	brain:	n/a
44	chr2:180886608-180886658	BE2_C	brain:	n/a
45	chr2:180875203-180875253	GM12892	blood:	n/a
46	chr2:180871809-180871859	AG09319	gingival:	n/a
47	chr2:180872142-180872192	HIPEpiC	eye:	n/a
48	chr2:180872053-180872103	HL-60	blood:	n/a
49	chr2:180875203-180875253	CMK	blood:	n/a
50	chr2:180921730-180921780	AG09309	skin:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr2:180899797..180902470-chr2:180903830..180906048,3	K562	blood:
2	chr2:181011027..181014182-chr2:181020328..181022944,3	K562	blood:
3	chr2:180869960..180872190-chr2:180885563..180889439,3	K562	blood:
4	chr2:180994987..180997418-chr2:180999723..181004072,3	K562	blood:
5	chr2:180863719..180867235-chr2:180869883..180873027,5	MCF-7	breast:
6	chr2:180687765..180690198-chr2:180866903..180869093,2	K562	blood:
7	chr2:180850802..180852751-chr2:180863607..180865249,2	MCF-7	breast:
8	chr2:180856164..180859331-chr2:180861905..180864411,3	K562	blood:
9	chr2:180853987..180858139-chr2:180866524..180870001,3	MCF-7	breast:
10	chr2:180868512..180871187-chr2:180902813..180905505,2	MCF-7	breast:
11	chr2:180650807..180652481-chr2:180868354..180871032,2	K562	blood:
12	chr2:180988723..180989602-chr2:182579889..182580461,2	K562	blood:
13	chr2:181008035..181010115-chr2:181024516..181027089,2	K562	blood:
14	chr2:180982648..180984525-chr2:181042501..181045377,2	K562	blood:
15	chr2:180869522..180873044-chr2:180927069..180929739,3	K562	blood:
16	chr2:180870527..180872087-chr2:181555247..181557318,2	K562	blood:
17	chr2:180995918..180998035-chr2:181001168..181004072,2	K562	blood:
18	chr2:180854973..180857186-chr2:180866635..180869075,2	MCF-7	breast:
19	chr2:180989111..180989829-chr2:181923203..181924094,3	K562	blood:
20	chr2:180974293..180977985-chr2:180978156..180981417,3	K562	blood:
21	chr2:180908544..180911277-chr2:180914469..180916339,2	K562	blood:
22	chr2:180869542..180871698-chr2:180887841..180889439,2	K562	blood:
23	chr2:180930245..180931845-chr2:180940075..180942522,2	K562	blood:
24	chr2:180974293..180977985-chr2:180978156..180981417,3	K562	blood:
25	chr2:180876562..180879495-chr2:180879895..180882049,2	K562	blood:
26	chr2:180868512..180871187-chr2:180902813..180905505,2	MCF-7	breast:
27	chr2:180856098..180856777-chr2:180941779..180942671,2	K562	blood:
28	chr2:180885627..180887178-chr2:180887295..180890213,2	K562	blood:
29	chr2:180928043..180930096-chr2:180936607..180939522,2	K562	blood:
30	chr2:180928043..180930096-chr2:180936607..180939522,2	K562	blood:
31	chr2:180865306..180867411-chr2:180884428..180886145,2	K562	blood:
32	chr2:180902516..180904628-chr2:180905527..180907773,2	K562	blood:
33	chr2:180286497..180287013-chr2:180941786..180942316,2	K562	blood:
34	chr2:180869542..180871698-chr2:180887841..180889439,2	K562	blood:
35	chr2:181008035..181010115-chr2:181024516..181027089,2	K562	blood:
36	chr2:180868081..180870113-chr2:205110359..205111860,2	K562	blood:
37	chr2:180885627..180887178-chr2:180887295..180890213,2	K562	blood:
38	chr2:180855717..180856981-chr2:180941679..180942512,4	MCF-7	breast:
39	chr2:180968132..180970625-chr2:181844216..181846742,2	K562	blood:
40	chr2:180854938..180857526-chr2:180942782..180945485,2	MCF-7	breast:
41	chr2:180937468..180939367-chr2:180965910..180967492,2	K562	blood:
42	chr2:180942168..180944671-chr2:180952127..180953902,2	K562	blood:
43	chr2:180865306..180867411-chr2:180884428..180886145,2	K562	blood:
44	chr2:180937468..180939367-chr2:180965910..180967492,2	K562	blood:
45	chr2:180995918..180998035-chr2:181001168..181004072,2	K562	blood:
46	chr2:181011027..181014182-chr2:181020328..181022944,3	K562	blood:
47	chr2:180989858..180990890-chr2:181922991..181924050,3	MCF-7	breast:
48	chr2:180870517..180873087-chr2:180873234..180875366,2	MCF-7	breast:
49	chr2:180908544..180911277-chr2:180914469..180916339,2	K562	blood:
50	chr2:180275260..180275773-chr2:180941931..180942644,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UBE2E3-7	chr2:180978905-180979485	l_2002_chr2:180978904-180986546_testes
2	lnc-UBE2E3-7	chr2:180986436-180986546	l_2002_chr2:180978904-180986546_testes

No data

Variant related genes	Relation type
CWC22	TF binding region
CWC22	CpG island
ENSG00000163510	chromatin interactions
ENSG00000225258	chromatin interactions
ENSG00000236153	chromatin interactions
ENSG00000170035	chromatin interactions

Extended variants
information (count: 4230 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:4230 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564194125	chr2:180864264-180864265	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs577715216	chr2:180864320-180864321	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189848298	chr2:180864372-180864373	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563329687	chr2:180864385-180864386	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114397210	chr2:180864386-180864387	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs367913639	chr2:180864387-180864388	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs548149590	chr2:180864413-180864414	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs182133312	chr2:180864423-180864424	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs375987279	chr2:180864447-180864448	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs527445160	chr2:180864619-180864620	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs547607154	chr2:180864666-180864667	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570700050	chr2:180864670-180864671	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs539524819	chr2:180864671-180864672	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs72962580	chr2:180864681-180864682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs111724388	chr2:180864696-180864697	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs550340964	chr2:180864710-180864711	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs552635624	chr2:180864711-180864712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs148432011	chr2:180864716-180864717	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs58408527	chr2:180864796-180864797	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs535170310	chr2:180864834-180864835	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs548691201	chr2:180864842-180864843	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535448794	chr2:180864901-180864902	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539794249	chr2:180864922-180864923	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs374710994	chr2:180864932-180864933	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs10497555	chr2:180864967-180864968	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs535056905	chr2:180864971-180864972	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs537203561	chr2:180865000-180865001	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186494964	chr2:180865046-180865047	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs543491334	chr2:180865120-180865121	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs373075001	chr2:180865132-180865133	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs116227566	chr2:180865133-180865134	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs573908318	chr2:180865177-180865178	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs191876954	chr2:180865208-180865209	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs183977793	chr2:180865256-180865257	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs142591665	chr2:180865368-180865369	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs566774467	chr2:180865387-180865388	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs188520206	chr2:180865415-180865416	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs564249964	chr2:180865427-180865428	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs193098938	chr2:180865468-180865469	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs549869527	chr2:180865485-180865486	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs182703049	chr2:180865494-180865495	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs186838456	chr2:180865497-180865498	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs199821429	chr2:180865559-180865560	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs548961015	chr2:180865590-180865591	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs146492738	chr2:180865599-180865600	Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs6744386	chr2:180865625-180865626	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191340967	chr2:180865632-180865633	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571481872	chr2:180865641-180865642	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs6760751	chr2:180865667-180865668	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577033032	chr2:180865687-180865688	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180809400-180871000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr2:180813400-180868200	Weak transcription	Stomach Mucosa	stomach
3	chr2:180816800-180868400	Weak transcription	Pancreas	Pancrea
4	chr2:180816800-180869000	Weak transcription	Spleen	Spleen
5	chr2:180816800-180870600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr2:180819000-180871000	Weak transcription	Esophagus	oesophagus
7	chr2:180823400-180870600	Weak transcription	Fetal Intestine Small	intestine
8	chr2:180829600-180871200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr2:180830800-180871000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
10	chr2:180836800-180870400	Weak transcription	A549	lung
11	chr2:180839800-180870400	Weak transcription	Rectal Smooth Muscle	rectum
12	chr2:180843000-180870200	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr2:180846800-180867000	Weak transcription	Colon Smooth Muscle	Colon
14	chr2:180846800-180869800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr2:180847600-180866200	Weak transcription	Psoas Muscle	Psoas
16	chr2:180849000-180869600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr2:180850600-180870800	Weak transcription	HSMMtube	muscle
18	chr2:180851000-180870200	Weak transcription	Hela-S3	cervix
19	chr2:180851600-180870400	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr2:180851800-180870400	Weak transcription	HUVEC	blood vessel
21	chr2:180852000-180865000	Weak transcription	Brain Cingulate Gyrus	brain
22	chr2:180852200-180870600	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr2:180853200-180868000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr2:180853600-180869600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr2:180856600-180870400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
26	chr2:180856800-180865400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr2:180857200-180870000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr2:180857200-180870400	Weak transcription	Brain Anterior Caudate	brain
29	chr2:180857200-180870400	Weak transcription	Thymus	Thymus
30	chr2:180857200-180871000	Weak transcription	Lung	lung
31	chr2:180857400-180865800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr2:180857600-180869800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr2:180857800-180866000	Weak transcription	Ovary	ovary
34	chr2:180857800-180867000	Weak transcription	Primary hematopoietic stem cells	blood
35	chr2:180857800-180867200	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr2:180857800-180867800	Weak transcription	Fetal Brain Female	brain
37	chr2:180857800-180870400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr2:180857800-180870400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr2:180857800-180870600	Weak transcription	NHLF	lung
40	chr2:180857800-180870800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr2:180857800-180870800	Weak transcription	Fetal Intestine Large	intestine
42	chr2:180858000-180865200	Weak transcription	HMEC	breast
43	chr2:180858000-180865200	Weak transcription	NHEK	skin
44	chr2:180858000-180866800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr2:180858000-180867200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr2:180858000-180868200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr2:180858000-180869000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr2:180858000-180869600	Weak transcription	Rectal Mucosa Donor 29	rectum
49	chr2:180858000-180869800	Weak transcription	Adipose Nuclei	Adipose
50	chr2:180858000-180869800	Weak transcription	Stomach Smooth Muscle	stomach

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