Variant report

Variant	nsv873631
Chromosome Location	chr2:9975557-10059770
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1536)
CpG islands
(count:672)
Chromatin interactive
region (count:124)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1536 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:10054894-10055193	K562	blood:	n/a	n/a
2	ARID3A	chr2:10036343-10036540	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:10029607-10030329	HepG2	liver:	n/a	n/a
4	ARID3A	chr2:9984441-9984472	K562	blood:	n/a	n/a
5	ARID3A	chr2:10052615-10052989	HepG2	liver:	n/a	n/a
6	ARID3A	chr2:9983018-9983738	K562	blood:	n/a	n/a
7	ARID3A	chr2:9983246-9983987	HepG2	liver:	n/a	n/a
8	ATF1	chr2:10054776-10055157	K562	blood:	n/a	n/a
9	ATF2	chr2:9983314-9984086	GM12878	blood:	n/a	n/a
10	ATF2	chr2:10054670-10055232	GM12878	blood:	n/a	n/a
11	ATF2	chr2:9984687-9985105	GM12878	blood:	n/a	n/a
12	ATF2	chr2:10054747-10055187	GM12878	blood:	n/a	n/a
13	ATF3	chr2:9983186-9983933	A549	lung:	n/a	n/a
14	ATF3	chr2:9983224-9984112	A549	lung:	n/a	n/a
15	ATF3	chr2:10054816-10055044	K562	blood:	n/a	n/a
16	ATF3	chr2:10054734-10055092	K562	blood:	n/a	n/a
17	BACH1	chr2:9984714-9984799	K562	blood:	n/a	n/a
18	BACH1	chr2:9983162-9984236	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr2:10054880-10055075	K562	blood:	n/a	n/a
20	BATF	chr2:9983221-9983529	GM12878	blood:	n/a	n/a
21	BATF	chr2:10054796-10055100	GM12878	blood:	n/a	n/a
22	BATF	chr2:10054687-10055086	GM12878	blood:	n/a	n/a
23	BATF	chr2:10037503-10037913	GM12878	blood:	n/a	chr2:10037722-10037733
24	BCL11A	chr2:10054773-10055070	GM12878	blood:	n/a	n/a
25	BCL3	chr2:10054744-10055096	GM12878	blood:	n/a	n/a
26	BCL3	chr2:9983036-9984445	A549	lung:	n/a	n/a
27	BCL3	chr2:9983343-9984305	A549	lung:	n/a	n/a
28	BCLAF1	chr2:9983137-9984285	GM12878	blood:	n/a	n/a
29	BCLAF1	chr2:9984584-9985043	GM12878	blood:	n/a	n/a
30	BCLAF1	chr2:10054741-10055071	GM12878	blood:	n/a	n/a
31	BHLHE40	chr2:10054509-10055197	K562	blood:	n/a	n/a
32	BHLHE40	chr2:9983167-9984338	GM12878	blood:	n/a	n/a
33	BHLHE40	chr2:9983145-9984338	K562	blood:	n/a	n/a
34	BHLHE40	chr2:10054533-10055280	GM12878	blood:	n/a	n/a
35	BHLHE40	chr2:10054761-10055119	A549	lung:	n/a	n/a
36	BHLHE40	chr2:10054804-10055053	HepG2	liver:	n/a	n/a
37	BHLHE40	chr2:9983333-9983969	HepG2	liver:	n/a	n/a
38	BRCA1	chr2:9983246-9983750	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr2:9983285-9983934	GM12878	blood:	n/a	n/a
40	BRCA1	chr2:10054772-10055123	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr2:10044919-10045008	Hela-S3	cervix:	n/a	n/a
42	BRCA1	chr2:9983418-9983831	HepG2	liver:	n/a	n/a
43	BRCA1	chr2:9983279-9984047	Hela-S3	cervix:	n/a	n/a
44	CBX3	chr2:9998428-9999134	K562	blood:	n/a	n/a
45	CBX3	chr2:9983511-9984012	K562	blood:	n/a	n/a
46	CBX3	chr2:10054734-10055156	K562	blood:	n/a	n/a
47	CBX3	chr2:9982631-9984462	K562	blood:	n/a	n/a
48	CBX3	chr2:10001188-10001598	K562	blood:	n/a	n/a
49	CBX3	chr2:10037449-10038076	HCT-116	colon:	n/a	n/a
50	CBX3	chr2:10054764-10055086	K562	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:9983052-9983102	HCT-116	colon:	n/a
2	chr2:9983052-9983102	HCT-116	colon:	n/a
3	chr2:9987440-9987490	Hela-S3	cervix:	n/a
4	chr2:9983052-9983102	HRPEpiC	eye:	n/a
5	chr2:10024636-10024686	IMR90	lung:	fetal
6	chr2:9984929-9984979	HepG2	liver:	n/a
7	chr2:9987440-9987490	BJ	skin:	n/a
8	chr2:9984929-9984979	AG10803	skin:	n/a
9	chr2:9987440-9987490	HRPEpiC	eye:	n/a
10	chr2:9984929-9984979	GM12878	blood:	n/a
11	chr2:9983052-9983102	PrEC	prostate:	n/a
12	chr2:9983859-9983909	SKMC	muscle:	n/a
13	chr2:9983211-9983261	SK-N-SH_RA	brain:	n/a
14	chr2:10054883-10054933	AG09309	skin:	n/a
15	chr2:9983427-9983477	SK-N-SH	brain:	n/a
16	chr2:9983427-9983477	BJ	skin:	n/a
17	chr2:9983859-9983909	ovcar-3	ovarian:	n/a
18	chr2:9983430-9983480	Jurkat	blood:	n/a
19	chr2:10054883-10054933	HCPEpiC	choroid plexus:	n/a
20	chr2:9984929-9984979	SAEC	small airway:	n/a
21	chr2:10024636-10024686	ProgFib	skin:	n/a
22	chr2:9984929-9984979	AoSMC	blood vessel:	n/a
23	chr2:10037561-10037611	ovcar-3	ovarian:	n/a
24	chr2:9983211-9983261	SKMC	muscle:	n/a
25	chr2:10054883-10054933	GM12891	blood:	n/a
26	chr2:9983859-9983909	U87	brain:	n/a
27	chr2:9983859-9983909	SK-N-SH	brain:	n/a
28	chr2:9983211-9983261	NB4	blood:	n/a
29	chr2:9983427-9983477	SK-N-MC	brain:	n/a
30	chr2:9983211-9983261	AG04449	skin:	fetal
31	chr2:9983094-9983144	H1-hESC	embryonic stem cell:	embryo
32	chr2:9983430-9983480	Caco-2	colon:	n/a
33	chr2:9984929-9984979	ECC-1	luminal epithelium:	n/a
34	chr2:9983859-9983909	Hepatocyte	liver:	n/a
35	chr2:9987440-9987490	HCT-116	colon:	n/a
36	chr2:10037561-10037611	PANC-1	pancreas:	n/a
37	chr2:9983094-9983144	AoSMC	blood vessel:	n/a
38	chr2:10054883-10054933	Hela-S3	cervix:	n/a
39	chr2:9983211-9983261	HEEpiC	esophagus:	n/a
40	chr2:9983094-9983144	HL-60	blood:	n/a
41	chr2:9983859-9983909	AG09319	gingival:	n/a
42	chr2:9987440-9987490	HAEpiC	amniotic membrane:	n/a
43	chr2:9983859-9983909	HCM	heart:	n/a
44	chr2:9983430-9983480	HEK293	kidney:	embryo
45	chr2:10037561-10037611	NT2-D1	testis:	n/a
46	chr2:9983094-9983144	IMR90	lung:	fetal
47	chr2:10037561-10037611	HUVEC	blood vessel:	n/a
48	chr2:9983427-9983477	AG09319	gingival:	n/a
49	chr2:10054883-10054933	IMR90	lung:	fetal
50	chr2:9983094-9983144	Caco-2	colon:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr2:10022528..10025369-chr2:10031502..10033505,2	K562	blood:
2	chr2:10023869..10026802-chr2:10030630..10033505,2	K562	blood:
3	chr2:10053405..10055914-chr2:10061703..10064557,2	K562	blood:
4	chr2:9986181..9988070-chr2:9991011..9993550,2	MCF-7	breast:
5	chr10:76969734..76970322-chr2:9983044..9983554,2	NB4	blood:
6	chr2:10039201..10042198-chr2:10045779..10048080,2	MCF-7	breast:
7	chr2:10037949..10040040-chr2:10055239..10057291,2	MCF-7	breast:
8	chr2:9983297..9984997-chr2:10260468..10262228,2	K562	blood:
9	chr2:9981404..9986079-chr2:9986481..9992681,8	MCF-7	breast:
10	chr12:92539579..92540096-chr2:9983233..9984120,2	NB4	blood:
11	chr2:10016465..10019089-chr2:10091206..10093388,2	MCF-7	breast:
12	chr2:9990181..9994001-chr2:9995377..9997163,3	MCF-7	breast:
13	chr2:10045993..10047524-chr2:10050988..10053341,2	K562	blood:
14	chr1:225117101..225117940-chr2:9982915..9983806,2	Hela-S3	cervix:
15	chr2:10055984..10058361-chr2:10061943..10063449,2	MCF-7	breast:
16	chr2:10045831..10047655-chr2:10091725..10093739,2	MCF-7	breast:
17	chr19:36605408..36606315-chr2:9983471..9984383,2	Hela-S3	cervix:
18	chr2:9985865..9987759-chr2:9990520..9994621,3	MCF-7	breast:
19	chr2:9983262..9985223-chr2:10260728..10263822,3	K562	blood:
20	chr2:9985747..9988019-chr2:10062440..10064881,2	MCF-7	breast:
21	chr2:10058951..10060878-chr2:10081099..10082615,2	K562	blood:
22	chr2:9982271..9985181-chr2:10090033..10093358,4	K562	blood:
23	chr2:9982957..9983900-chr3:149530307..149531181,2	Hela-S3	cervix:
24	chr2:10045993..10047524-chr2:10050988..10053341,2	K562	blood:
25	chr2:9939991..9942900-chr2:10036080..10038755,2	MCF-7	breast:
26	chr2:9981933..9984802-chr2:10182812..10185710,3	K562	blood:
27	chr2:9901947..9904351-chr2:9980319..9983166,2	K562	blood:
28	chr2:9983066..9987186-chr2:10091615..10095343,4	MCF-7	breast:
29	chr2:10049796..10051308-chr2:10053649..10056131,2	K562	blood:
30	chr12:4757537..4758351-chr2:9983167..9983703,2	Hela-S3	cervix:
31	chr2:9971442..9974071-chr2:9977767..9979870,2	MCF-7	breast:
32	chr2:10035308..10037799-chr2:10038582..10040182,2	MCF-7	breast:
33	chr2:10032485..10035098-chr2:10036586..10038853,2	K562	blood:
34	chr2:10013311..10015489-chr2:10017066..10019345,2	MCF-7	breast:
35	chr2:9988819..9991090-chr2:9993199..9995026,2	MCF-7	breast:
36	chr2:10036313..10038528-chr2:10044301..10045845,2	MCF-7	breast:
37	chr2:10015734..10018207-chr2:10020455..10022125,2	K562	blood:
38	chr2:10019152..10020684-chr2:10028239..10030255,2	MCF-7	breast:
39	chr2:9984016..9986818-chr2:10112280..10114129,2	MCF-7	breast:
40	chr2:9982784..9985771-chr2:10027787..10030557,2	MCF-7	breast:
41	chr2:9936512..9939080-chr2:9983882..9985731,2	MCF-7	breast:
42	chr2:10025374..10028699-chr2:10030128..10032449,3	MCF-7	breast:
43	chr2:10053405..10055914-chr2:10061703..10065567,3	K562	blood:
44	chr2:9988516..9990339-chr2:9992824..9994417,2	MCF-7	breast:
45	chr2:9983243..9984795-chr2:10042473..10044081,2	K562	blood:
46	chr2:10006138..10008945-chr2:10011171..10013813,2	K562	blood:
47	chr2:10036313..10038528-chr2:10044301..10045845,2	MCF-7	breast:
48	chr2:10019152..10020684-chr2:10028239..10030255,2	MCF-7	breast:
49	chr2:9981748..9983787-chr2:10179341..10181254,2	K562	blood:
50	chr2:10023869..10026802-chr2:10030630..10033505,2	K562	blood:

No data

Variant related genes	Relation type
TAF1B	TF binding region
TAF1B	CpG island
ENSG00000139180	chromatin interactions
ENSG00000167460	chromatin interactions
ENSG00000115758	chromatin interactions
ENSG00000134317	chromatin interactions
ENSG00000165637	chromatin interactions
ENSG00000185842	chromatin interactions
ENSG00000105258	chromatin interactions
ENSG00000245904	chromatin interactions
ENSG00000133639	chromatin interactions
ENSG00000130164	chromatin interactions
ENSG00000171848	chromatin interactions
ENSG00000105254	chromatin interactions
ENSG00000260077	chromatin interactions
ENSG00000272524	chromatin interactions
ENSG00000127526	chromatin interactions
ENSG00000257135	chromatin interactions
ENSG00000111254	chromatin interactions
ENSG00000206633	chromatin interactions
ENSG00000082996	chromatin interactions
ENSG00000172059	chromatin interactions
ENSG00000115750	chromatin interactions

Extended variants
information (count: 3309 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3309 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7568330	chr2:9975557-9975558	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187401867	chr2:9975652-9975653	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs7580521	chr2:9975684-9975685	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs538291766	chr2:9975703-9975704	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs529599760	chr2:9975742-9975743	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs546211229	chr2:9975762-9975763	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs80336909	chr2:9975774-9975775	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs191851067	chr2:9975777-9975778	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs534207789	chr2:9975857-9975858	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs139342351	chr2:9975908-9975909	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs78420122	chr2:9975911-9975912	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532268510	chr2:9975989-9975990	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs77060524	chr2:9975992-9975993	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs79276033	chr2:9975997-9975998	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs569479518	chr2:9976129-9976130	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs372394876	chr2:9976145-9976146	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs80238678	chr2:9976182-9976183	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs184588961	chr2:9976185-9976186	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576608314	chr2:9976196-9976197	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs80295189	chr2:9976225-9976226	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs565264662	chr2:9976266-9976267	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs116604962	chr2:9976275-9976276	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs189620125	chr2:9976389-9976390	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs145038862	chr2:9976409-9976410	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs561145875	chr2:9976421-9976422	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs542938140	chr2:9976425-9976426	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs185802874	chr2:9976501-9976502	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs114101112	chr2:9976517-9976518	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs76624418	chr2:9976518-9976519	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs532060784	chr2:9976557-9976558	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190330552	chr2:9976580-9976581	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs56049203	chr2:9976582-9976583	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs78852899	chr2:9976585-9976586	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs4669469	chr2:9976593-9976594	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs181781336	chr2:9976600-9976601	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs534524978	chr2:9976629-9976630	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554132510	chr2:9976667-9976668	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs567854635	chr2:9976716-9976717	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs536493243	chr2:9976744-9976745	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs375874722	chr2:9976786-9976787	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs556785768	chr2:9976792-9976793	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs576646090	chr2:9976799-9976800	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs545497256	chr2:9976835-9976836	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs559006758	chr2:9976852-9976853	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs572309628	chr2:9976855-9976856	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs77673827	chr2:9976857-9976858	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs185962767	chr2:9976864-9976865	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs561072742	chr2:9976931-9976932	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs6707020	chr2:9976964-9976965	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs543246445	chr2:9976965-9976966	Enhancers Weak transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Breast cancer	17133270	CNVD
Mental retardation	17847001	CNVD
Glioblastoma multiforme	21080181	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Cancer	20164920	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Glioma	17123091	CNVD
Breast cancer	20409316	CNVD
Multiple myeloma	16616336	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Neuroblastoma	18923524	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:2808 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:9955200-9983000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr2:9971600-9976400	Weak transcription	Hela-S3	cervix
3	chr2:9972000-9976600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr2:9972600-9976400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr2:9972600-9983000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:9972800-9976200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr2:9972800-9976800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr2:9973000-9976400	Weak transcription	Osteobl	bone
9	chr2:9973000-9976600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr2:9973000-9976800	Weak transcription	HMEC	breast
11	chr2:9973000-9976800	Weak transcription	NHEK	skin
12	chr2:9973000-9977000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:9973200-9976600	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr2:9973400-9976400	Weak transcription	Placenta	Placenta
15	chr2:9973600-9976400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr2:9973800-9976400	Weak transcription	NHDF-Ad	bronchial
17	chr2:9974200-9976200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr2:9976200-9978000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:9976200-9978000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr2:9976200-9978000	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr2:9976400-9976800	Enhancers	Hela-S3	cervix
22	chr2:9976400-9977000	Enhancers	Adipose Nuclei	Adipose
23	chr2:9976400-9977200	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr2:9976400-9977200	Enhancers	Skeletal Muscle Female	skeletal muscle
25	chr2:9976400-9977800	Enhancers	NHDF-Ad	bronchial
26	chr2:9976400-9977800	Enhancers	Osteobl	bone
27	chr2:9976400-9978000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr2:9976400-9979800	Enhancers	Placenta	Placenta
29	chr2:9976600-9977000	Enhancers	Psoas Muscle	Psoas
30	chr2:9976600-9977200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:9976600-9977600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr2:9976600-9977600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr2:9976600-9977600	Enhancers	Placenta Amnion	Placenta Amnion
34	chr2:9976600-9977800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:9976600-9977800	Enhancers	Muscle Satellite Cultured Cells	--
36	chr2:9976600-9977800	Enhancers	HSMM	muscle
37	chr2:9976600-9977800	Enhancers	HSMMtube	muscle
38	chr2:9976800-9977200	Flanking Active TSS	Hela-S3	cervix
39	chr2:9976800-9977200	Enhancers	K562	blood
40	chr2:9976800-9977600	Enhancers	HepG2	liver
41	chr2:9976800-9977800	Enhancers	NHLF	lung
42	chr2:9976800-9978000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr2:9976800-9978000	Enhancers	HMEC	breast
44	chr2:9976800-9978000	Enhancers	NHEK	skin
45	chr2:9977000-9977600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:9977000-9983000	Weak transcription	Adipose Nuclei	Adipose
47	chr2:9977200-9977800	Enhancers	Hela-S3	cervix
48	chr2:9977200-9978000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr2:9977200-9982600	Weak transcription	K562	blood
50	chr2:9977200-9983000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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