Variant report

Variant	nsv1024770
Chromosome Location	chr7:38357075-38387431
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1562)
CpG islands
(count:794)
Chromatin interactive
region (count:26)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1562 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:38375261-38375775	K562	blood:	n/a	n/a
2	ARID3A	chr7:38380924-38381236	K562	blood:	n/a	n/a
3	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
4	ATF1	chr7:38358478-38358765	K562	blood:	n/a	n/a
5	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
6	ATF1	chr7:38375958-38376139	K562	blood:	n/a	n/a
7	ATF1	chr7:38375268-38375593	K562	blood:	n/a	n/a
8	ATF2	chr7:38375126-38375565	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr7:38375154-38375534	GM12878	blood:	n/a	n/a
10	ATF2	chr7:38358345-38358831	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr7:38375159-38375625	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:38375250-38375572	K562	blood:	n/a	n/a
13	BACH1	chr7:38371330-38371815	H1-hESC	embryonic stem cell:	n/a	chr7:38371628-38371642
14	BACH1	chr7:38375296-38375468	K562	blood:	n/a	n/a
15	BATF	chr7:38375071-38375552	GM12878	blood:	n/a	n/a
16	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
17	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
18	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
19	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
20	BCL3	chr7:38375082-38375686	A549	lung:	n/a	chr7:38375198-38375207
21	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
22	BCLAF1	chr7:38375115-38375667	GM12878	blood:	n/a	chr7:38375198-38375207
23	BCLAF1	chr7:38375138-38375654	GM12878	blood:	n/a	chr7:38375198-38375207
24	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
25	BHLHE40	chr7:38358558-38358736	K562	blood:	n/a	n/a
26	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
27	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
28	BHLHE40	chr7:38374979-38376051	K562	blood:	n/a	n/a
29	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
30	BHLHE40	chr7:38370489-38370864	K562	blood:	n/a	n/a
31	BHLHE40	chr7:38375174-38375547	GM12878	blood:	n/a	n/a
32	BRCA1	chr7:38375364-38375495	HepG2	liver:	n/a	n/a
33	CBX3	chr7:38380733-38381387	K562	blood:	n/a	n/a
34	CBX3	chr7:38370432-38370850	K562	blood:	n/a	n/a
35	CBX3	chr7:38380820-38381270	K562	blood:	n/a	n/a
36	CBX3	chr7:38375149-38375641	K562	blood:	n/a	n/a
37	CBX3	chr7:38375046-38375715	K562	blood:	n/a	n/a
38	CCNT2	chr7:38375300-38375668	K562	blood:	n/a	n/a
39	CCNT2	chr7:38380858-38381223	K562	blood:	n/a	n/a
40	CEBPB	chr7:38361024-38361459	IMR90	lung:	n/a	chr7:38361262-38361275
41	CEBPB	chr7:38380943-38381315	K562	blood:	n/a	n/a
42	CEBPB	chr7:38357963-38358244	ECC-1	luminal epithelium:	n/a	chr7:38358095-38358108
43	CEBPB	chr7:38358105-38358116	K562	blood:	n/a	n/a
44	CEBPB	chr7:38357938-38358233	H1-hESC	embryonic stem cell:	n/a	chr7:38358095-38358108
45	CEBPB	chr7:38375195-38375630	K562	blood:	n/a	n/a
46	CEBPB	chr7:38375302-38375655	K562	blood:	n/a	n/a
47	CEBPD	chr7:38380772-38381308	K562	blood:	n/a	n/a
48	CHD1	chr7:38360726-38361756	IMR90	lung:	n/a	n/a
49	CHD1	chr7:38375229-38375562	GM12878	blood:	n/a	n/a
50	CHD2	chr7:38375308-38375663	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38357684-38357734	MCF10A-Er-Src	breast:	n/a
2	chr7:38357684-38357734	MCF10A-Er-Src	breast:	n/a
3	chr7:38370988-38371038	Hela-S3	cervix:	n/a
4	chr7:38375376-38375426	ProgFib	skin:	n/a
5	chr7:38358429-38358479	K562	blood:	n/a
6	chr7:38370988-38371038	MCF-7	breast:	n/a
7	chr7:38375485-38375535	HEK293	kidney:	embryo
8	chr7:38370664-38370714	IMR90	lung:	fetal
9	chr7:38370676-38370726	MCF10A-Er-Src	breast:	n/a
10	chr7:38375485-38375535	ProgFib	skin:	n/a
11	chr7:38370988-38371038	SK-N-MC	brain:	n/a
12	chr7:38375485-38375535	A549	lung:	n/a
13	chr7:38357047-38357097	AG09319	gingival:	n/a
14	chr7:38375485-38375535	HPAEpiC	pulmonary alveolar:	n/a
15	chr7:38358683-38358733	HUVEC	blood vessel:	n/a
16	chr7:38370664-38370714	AG09319	gingival:	n/a
17	chr7:38361199-38361249	AG04449	skin:	fetal
18	chr7:38361199-38361249	AG09309	skin:	n/a
19	chr7:38370988-38371038	Caco-2	colon:	n/a
20	chr7:38361199-38361249	AG04450	lung:	fetal
21	chr7:38358429-38358479	NHDF-neo	bronchial:	n/a
22	chr7:38370664-38370714	HRCEpiC	kidney:	n/a
23	chr7:38358683-38358733	IMR90	lung:	fetal
24	chr7:38357684-38357734	HCM	heart:	n/a
25	chr7:38375485-38375535	NHBE	bronchial:	n/a
26	chr7:38380487-38380537	HEEpiC	esophagus:	n/a
27	chr7:38358683-38358733	HCT-116	colon:	n/a
28	chr7:38375485-38375535	SK-N-MC	brain:	n/a
29	chr7:38375376-38375426	MCF-7	breast:	n/a
30	chr7:38361199-38361249	U87	brain:	n/a
31	chr7:38375376-38375426	NH-A	brain:	n/a
32	chr7:38370874-38370924	HL-60	blood:	n/a
33	chr7:38370664-38370714	ECC-1	luminal epithelium:	n/a
34	chr7:38380582-38380632	HCT-116	colon:	n/a
35	chr7:38358683-38358733	HIPEpiC	eye:	n/a
36	chr7:38358429-38358479	MCF-7	breast:	n/a
37	chr7:38375376-38375426	RPTEC	kidney:	n/a
38	chr7:38380487-38380537	SKMC	muscle:	n/a
39	chr7:38358429-38358479	ProgFib	skin:	n/a
40	chr7:38370988-38371038	HL-60	blood:	n/a
41	chr7:38375485-38375535	GM12891	blood:	n/a
42	chr7:38361199-38361249	PANC-1	pancreas:	n/a
43	chr7:38370676-38370726	BJ	skin:	n/a
44	chr7:38361199-38361249	RPTEC	kidney:	n/a
45	chr7:38375376-38375426	GM12891	blood:	n/a
46	chr7:38370664-38370714	HEEpiC	esophagus:	n/a
47	chr7:38370988-38371038	ECC-1	luminal epithelium:	n/a
48	chr7:38370676-38370726	SKMC	muscle:	n/a
49	chr7:38357684-38357734	K562	blood:	n/a
50	chr7:38380582-38380632	HRE	kidney:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38378957..38381571-chr7:38387227..38389473,2	K562	blood:
2	chr7:38146965..38147587-chr7:38385316..38385987,2	MCF-7	breast:
3	chr7:38269978..38272526-chr7:38377435..38379545,2	K562	blood:
4	chr7:38378347..38380949-chr7:38392502..38394879,2	K562	blood:
5	chr7:38379860..38381671-chr7:38382000..38383618,2	K562	blood:
6	chr7:38350441..38353889-chr7:38368470..38373744,5	K562	blood:
7	chr7:38380741..38382401-chr7:38383649..38386131,2	K562	blood:
8	chr7:37940728..37941537-chr7:38358496..38359055,2	MCF-7	breast:
9	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
10	chr7:38350491..38353138-chr7:38373860..38375500,2	K562	blood:
11	chr7:38350491..38352001-chr7:38373860..38376555,2	K562	blood:
12	chr7:38383736..38385810-chr7:38388077..38391054,2	MCF-7	breast:
13	chr7:38375472..38376033-chr7:38384935..38385704,2	MCF-7	breast:
14	chr7:38372590..38377698-chr7:38377994..38383669,12	K562	blood:
15	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
16	chr7:38369664..38372472-chr7:38373590..38376789,3	K562	blood:
17	chr7:38145396..38146142-chr7:38358527..38359113,2	MCF-7	breast:
18	chr7:38365694..38367640-chr7:38368298..38369847,2	K562	blood:
19	chr7:38268103..38269784-chr7:38382757..38385051,2	K562	blood:
20	chr7:38369534..38372460-chr7:38378778..38381886,3	K562	blood:
21	chr7:38357958..38360447-chr7:38360808..38363317,4	K562	blood:
22	chr7:38357958..38360447-chr7:38360808..38363317,4	K562	blood:
23	chr7:38385094..38385817-chr7:38407469..38408173,2	MCF-7	breast:
24	chr7:38255022..38255645-chr7:38375302..38376120,3	MCF-7	breast:
25	chr7:38375070..38375771-chr7:38393808..38394547,2	MCF-7	breast:
26	chr7:38369664..38372472-chr7:38373590..38376789,3	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38381098-38381400	NONHSAT120178
2	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
3	lnc-AMPH-7	chr7:38362047-38362331	NONHSAT120176
4	lnc-STARD3NL-1	chr7:38381216-38381400	ENSG00000250924
5	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
6	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
7	lnc-AMPH-6	chr7:38368841-38369244	ENSG00000272908.1
8	lnc-AMPH-6	chr7:38365671-38367234	ENSG00000272908.1
9	lnc-STARD3NL-1	chr7:38381747-38382154	NONHSAT120178
10	lnc-AMPH-5	chr7:38374642-38374951	NONHSAT120177
11	lnc-AMPH-5	chr7:38375073-38375115	NONHSAT120177
12	lnc-STARD3NL-1	chr7:38381178-38381400	NONHSAT120179

No data

Variant related genes	Relation type
ENSG00000272908	TF binding region
TRGV7	TF binding region
TRGV6	TF binding region
TRGVA	TF binding region
TRGV9	TF binding region
TRGV8	TF binding region
TRGV5P	TF binding region
ENSG00000272908	CpG island
TRGV7	CpG island
TRGV6	CpG island
TRGVA	CpG island
TRGV9	CpG island
TRGV8	CpG island
TRGV5P	CpG island
ENSG00000211696	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000249978	chromatin interactions
ENSG00000225992	chromatin interactions
ENSG00000272908	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000211695	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000211698	chromatin interactions
SERTAD3	miRNA target sites
CA13	miRNA target sites

Extended variants
information (count: 1459 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11769443	chr7:38357075-38357076	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs561644414	chr7:38357076-38357077	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs369893658	chr7:38357116-38357117	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs58848448	chr7:38357120-38357121	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs541047040	chr7:38357121-38357122	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs184979802	chr7:38357147-38357148	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs368857948	chr7:38357148-38357149	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs373605177	chr7:38357164-38357165	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs11980080	chr7:38357194-38357195	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs549909939	chr7:38357235-38357236	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs569792981	chr7:38357285-38357286	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs11765884	chr7:38357323-38357324	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548422833	chr7:38357331-38357332	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs568098197	chr7:38357374-38357375	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs371319033	chr7:38357395-38357396	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs77242858	chr7:38357408-38357409	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs553753128	chr7:38357475-38357476	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs2534564	chr7:38357498-38357499	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs75151088	chr7:38357499-38357500	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs556713252	chr7:38357501-38357502	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs576586896	chr7:38357566-38357567	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs74584661	chr7:38357606-38357607	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs555465469	chr7:38357619-38357620	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs150606979	chr7:38357620-38357621	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs540982105	chr7:38357633-38357634	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs564082558	chr7:38357675-38357676	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs115264213	chr7:38357685-38357686	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs552047716	chr7:38357713-38357714	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs563477874	chr7:38357754-38357755	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs369171260	chr7:38357796-38357797	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs529111016	chr7:38357830-38357831	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs548782624	chr7:38357838-38357839	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs189712633	chr7:38357860-38357861	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs527789159	chr7:38357862-38357863	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs547376881	chr7:38357875-38357876	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs139680694	chr7:38357880-38357881	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs556558841	chr7:38357909-38357910	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs149781003	chr7:38357923-38357924	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs570341337	chr7:38357924-38357925	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs183086525	chr7:38357940-38357941	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs34137670	chr7:38357998-38357999	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs116104768	chr7:38358068-38358069	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576216421	chr7:38358085-38358086	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2240844	chr7:38358102-38358103	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs150221989	chr7:38358156-38358157	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371087259	chr7:38358175-38358176	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs576811756	chr7:38358191-38358192	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs541110477	chr7:38358212-38358213	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs376281435	chr7:38358216-38358217	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs2534565	chr7:38358227-38358228	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
Renal cell carcinoma	18765545	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	18632612	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute myeloid leukemia	17237825	CNVD
Breast cancer	17899364	CNVD
Breast cancer	20409316	CNVD
Acute monocytic leukemia	16498392	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Sezary syndrome	18413736	CNVD
Gastric cancer	24379144	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:813 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38350400-38357200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr7:38351400-38358000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:38351400-38358400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr7:38351600-38358600	Weak transcription	Fetal Kidney	kidney
5	chr7:38351600-38358800	Enhancers	Primary neutrophils fromperipheralblood	blood
6	chr7:38351600-38363800	Weak transcription	Right Atrium	heart
7	chr7:38352000-38358200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr7:38353000-38357200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr7:38353000-38357200	Weak transcription	Fetal Muscle Leg	muscle
10	chr7:38353000-38358000	Weak transcription	Spleen	Spleen
11	chr7:38353000-38358000	Weak transcription	HUVEC	blood vessel
12	chr7:38353000-38358200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
13	chr7:38353000-38358200	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr7:38353000-38358600	Enhancers	Primary hematopoietic stem cells	blood
15	chr7:38353000-38359000	Weak transcription	GM12878-XiMat	blood
16	chr7:38353000-38360800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr7:38353200-38357400	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr7:38353200-38357400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr7:38353200-38357600	Weak transcription	Adipose Nuclei	Adipose
20	chr7:38353200-38358200	Weak transcription	Primary T helper cells PMA-I stimulated	--
21	chr7:38353200-38358600	Weak transcription	Primary T cells from cord blood	blood
22	chr7:38353600-38357400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:38353600-38360800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr7:38354800-38358400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:38355600-38358600	Enhancers	Placenta	Placenta
26	chr7:38355600-38358800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr7:38355800-38359000	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr7:38356200-38357200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
29	chr7:38356200-38357600	Weak transcription	Fetal Stomach	stomach
30	chr7:38356400-38357800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr7:38356600-38357200	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr7:38356600-38357400	Active TSS	Thymus	Thymus
33	chr7:38356600-38357800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr7:38356600-38358200	Active TSS	Primary T cells fromperipheralblood	blood
35	chr7:38356600-38358800	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr7:38356800-38357200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chr7:38356800-38357800	Flanking Active TSS	Fetal Thymus	thymus
38	chr7:38357000-38358000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr7:38357000-38358400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr7:38357000-38359200	Enhancers	Primary B cells from cord blood	blood
41	chr7:38357200-38357600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:38357200-38357600	Active TSS	Primary T helper naive cells from peripheral blood	blood
43	chr7:38357200-38357600	Enhancers	Duodenum Mucosa	Duodenum
44	chr7:38357200-38358400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr7:38357200-38358400	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
46	chr7:38357200-38358600	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
47	chr7:38357200-38358600	Enhancers	Fetal Muscle Leg	muscle
48	chr7:38357200-38359200	Enhancers	ES-I3 Cell Line	embryonic stem cell
49	chr7:38357400-38357600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
50	chr7:38357400-38357600	Enhancers	Sigmoid Colon	Sigmoid Colon

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