Variant report

Variant	nsv1033238
Chromosome Location	chr7:38356595-38400945
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2311)
CpG islands
(count:1282)
Chromatin interactive
region (count:29)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2311 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

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	chr7:38358478-38358765	K562	blood:	n/a	n/a
4	ATF1	chr7:38375958-38376139	K562	blood:	n/a	n/a
5	ATF1	chr7:38375268-38375593	K562	blood:	n/a	n/a
6	ATF1	chr7:38389490-38389669	K562	blood:	n/a	n/a
7	ATF1	chr7:38380742-38381291	K562	blood:	n/a	n/a
8	ATF1	chr7:38379898-38380061	K562	blood:	n/a	n/a
9	ATF2	chr7:38358345-38358831	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr7:38375154-38375534	GM12878	blood:	n/a	n/a
11	ATF2	chr7:38375126-38375565	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr7:38375250-38375572	K562	blood:	n/a	n/a
13	ATF3	chr7:38375159-38375625	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr7:38375296-38375468	K562	blood:	n/a	n/a
15	BACH1	chr7:38371330-38371815	H1-hESC	embryonic stem cell:	n/a	chr7:38371628-38371642
16	BATF	chr7:38393104-38393312	GM12878	blood:	n/a	n/a
17	BATF	chr7:38389336-38389771	GM12878	blood:	n/a	n/a
18	BATF	chr7:38398491-38398925	GM12878	blood:	n/a	n/a
19	BATF	chr7:38397936-38398227	GM12878	blood:	n/a	n/a
20	BATF	chr7:38388801-38389033	GM12878	blood:	n/a	n/a
21	BATF	chr7:38375071-38375552	GM12878	blood:	n/a	n/a
22	BATF	chr7:38388739-38389137	GM12878	blood:	n/a	n/a
23	BATF	chr7:38393728-38393936	GM12878	blood:	n/a	n/a
24	BATF	chr7:38385112-38385446	GM12878	blood:	n/a	n/a
25	BATF	chr7:38393104-38393355	GM12878	blood:	n/a	n/a
26	BATF	chr7:38397831-38398310	GM12878	blood:	n/a	n/a
27	BATF	chr7:38384447-38384746	GM12878	blood:	n/a	n/a
28	BATF	chr7:38384403-38384723	GM12878	blood:	n/a	n/a
29	BCL11A	chr7:38398493-38398682	GM12878	blood:	n/a	n/a
30	BCL11A	chr7:38384321-38384734	GM12878	blood:	n/a	chr7:38384540-38384549
31	BCL11A	chr7:38393701-38393947	GM12878	blood:	n/a	n/a
32	BCL11A	chr7:38397653-38398122	GM12878	blood:	n/a	chr7:38398022-38398031
33	BCL3	chr7:38375082-38375686	A549	lung:	n/a	chr7:38375198-38375207
34	BCLAF1	chr7:38375138-38375654	GM12878	blood:	n/a	chr7:38375198-38375207
35	BCLAF1	chr7:38389556-38389732	GM12878	blood:	n/a	n/a
36	BCLAF1	chr7:38385200-38385540	GM12878	blood:	n/a	n/a
37	BCLAF1	chr7:38375115-38375667	GM12878	blood:	n/a	chr7:38375198-38375207
38	BHLHE40	chr7:38375174-38375547	GM12878	blood:	n/a	n/a
39	BHLHE40	chr7:38389643-38389696	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:38398804-38399002	K562	blood:	n/a	n/a
41	BHLHE40	chr7:38379902-38380060	K562	blood:	n/a	n/a
42	BHLHE40	chr7:38385297-38385497	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:38393917-38394132	K562	blood:	n/a	n/a
44	BHLHE40	chr7:38380767-38381281	K562	blood:	n/a	n/a
45	BHLHE40	chr7:38358558-38358736	K562	blood:	n/a	n/a
46	BHLHE40	chr7:38385332-38385486	K562	blood:	n/a	n/a
47	BHLHE40	chr7:38374979-38376051	K562	blood:	n/a	n/a
48	BHLHE40	chr7:38370489-38370864	K562	blood:	n/a	n/a
49	BRCA1	chr7:38375364-38375495	HepG2	liver:	n/a	n/a
50	CBX3	chr7:38375046-38375715	K562	blood:	n/a	n/a

(count:1282 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38357047-38357097	GM12878	blood:	n/a
2	chr7:38357047-38357097	GM12878	blood:	n/a
3	chr7:38370664-38370714	AG04450	lung:	fetal
4	chr7:38356808-38356858	CMK	blood:	n/a
5	chr7:38357047-38357097	PFSK-1	brain:	n/a
6	chr7:38356865-38356915	NH-A	brain:	n/a
7	chr7:38358429-38358479	Hepatocyte	liver:	n/a
8	chr7:38358429-38358479	HMEC	breast:	n/a
9	chr7:38389659-38389709	SKMC	muscle:	n/a
10	chr7:38358429-38358479	HCF	heart:	n/a
11	chr7:38356808-38356858	AG09309	skin:	n/a
12	chr7:38375485-38375535	HCT-116	colon:	n/a
13	chr7:38380487-38380537	PFSK-1	brain:	n/a
14	chr7:38389991-38390041	PrEC	prostate:	n/a
15	chr7:38370874-38370924	HepG2	liver:	n/a
16	chr7:38356808-38356858	NH-A	brain:	n/a
17	chr7:38358429-38358479	BJ	skin:	n/a
18	chr7:38389685-38389735	HRCEpiC	kidney:	n/a
19	chr7:38356729-38356779	ProgFib	skin:	n/a
20	chr7:38358683-38358733	HUVEC	blood vessel:	n/a
21	chr7:38370676-38370726	HPAEpiC	pulmonary alveolar:	n/a
22	chr7:38398839-38398889	K562	blood:	n/a
23	chr7:38389685-38389735	H1-hESC	embryonic stem cell:	embryo
24	chr7:38370676-38370726	AG04449	skin:	fetal
25	chr7:38380582-38380632	HIPEpiC	eye:	n/a
26	chr7:38358429-38358479	RPTEC	kidney:	n/a
27	chr7:38370988-38371038	PANC-1	pancreas:	n/a
28	chr7:38370874-38370924	NHDF-neo	bronchial:	n/a
29	chr7:38356808-38356858	Hela-S3	cervix:	n/a
30	chr7:38370664-38370714	Hela-S3	cervix:	n/a
31	chr7:38357684-38357734	GM12892	blood:	n/a
32	chr7:38370664-38370714	MCF10A-Er-Src	breast:	n/a
33	chr7:38361199-38361249	A549	lung:	n/a
34	chr7:38375485-38375535	HCF	heart:	n/a
35	chr7:38389685-38389735	HL-60	blood:	n/a
36	chr7:38358429-38358479	HUVEC	blood vessel:	n/a
37	chr7:38356808-38356858	AG09319	gingival:	n/a
38	chr7:38389659-38389709	AG09309	skin:	n/a
39	chr7:38356808-38356858	K562	blood:	n/a
40	chr7:38389991-38390041	HCF	heart:	n/a
41	chr7:38357684-38357734	SAEC	small airway:	n/a
42	chr7:38361199-38361249	T-47D	breast:	n/a
43	chr7:38356729-38356779	ECC-1	luminal epithelium:	n/a
44	chr7:38357684-38357734	SKMC	muscle:	n/a
45	chr7:38356865-38356915	SK-N-SH_RA	brain:	n/a
46	chr7:38357684-38357734	Hepatocyte	liver:	n/a
47	chr7:38370874-38370924	HEEpiC	esophagus:	n/a
48	chr7:38370676-38370726	PrEC	prostate:	n/a
49	chr7:38389659-38389709	Caco-2	colon:	n/a
50	chr7:38389659-38389709	HRPEpiC	eye:	n/a

(count:29 , 50 per page) page: 1

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

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STARD3NL-1	chr7:38381747-38382154	NONHSAT120178
2	lnc-STARD3NL-1	chr7:38381216-38381400	ENSG00000250924
3	lnc-AMPH-10	chr7:38356616-38356709	NONHSAT120169
4	lnc-AMPH-6	chr7:38365671-38367234	ENSG00000272908.1
5	lnc-AMPH-4	chr7:38394799-38395026	NONHSAT120180
6	lnc-STARD3NL-1	chr7:38381683-38384763	ucscGeneNc_uc003tgp_1
7	lnc-STARD3NL-1	chr7:38389947-38390051	NONHSAT120179
8	lnc-AMPH-3	chr7:38395172-38395463	NONHSAT120181
9	lnc-AMPH-7	chr7:38362047-38362331	NONHSAT120176
10	lnc-STARD3NL-4	chr7:38400418-38400732	NONHSAT120183
11	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120161
12	lnc-STARD3NL-1	chr7:38385622-38385728	ENSG00000250924
13	lnc-AMPH-10	chr7:38356621-38356709	NONHSAT120162
14	lnc-STARD3NL-1	chr7:38381098-38381400	NONHSAT120178
15	lnc-AMPH-6	chr7:38368841-38369244	ENSG00000272908.1
16	lnc-STARD3NL-1	chr7:38389947-38390051	ENSG00000250924
17	lnc-STARD3NL-3	chr7:38397521-38397735	NONHSAT120182
18	lnc-STARD3NL-1	chr7:38381178-38381400	NONHSAT120179
19	lnc-STARD3NL-1	chr7:38385622-38385728	NONHSAT120179
20	lnc-AMPH-10	chr7:38356605-38356709	NONHSAT120166
21	lnc-AMPH-10	chr7:38356622-38356709	NONHSAT120167
22	lnc-AMPH-5	chr7:38374642-38374951	NONHSAT120177
23	lnc-AMPH-5	chr7:38375073-38375115	NONHSAT120177
24	lnc-AMPH-10	chr7:38356623-38356709	NONHSAT120170

No data

Variant related genes	Relation type
ENSG00000272908	TF binding region
TRGV7	TF binding region
TRGV5	TF binding region
TRGV6	TF binding region
TRGV4	TF binding region
TRGV3	TF binding region
TRGV8	TF binding region
TRGVA	TF binding region
TRGV9	TF binding region
TRGV5P	TF binding region
ENSG00000272908	CpG island
TRGV7	CpG island
TRGV5	CpG island
TRGV6	CpG island
TRGV4	CpG island
TRGV3	CpG island
TRGV8	CpG island
TRGVA	CpG island
TRGV9	CpG island
TRGV5P	CpG island
ENSG00000211698	chromatin interactions
ENSG00000211697	chromatin interactions
ENSG00000272908	chromatin interactions
ENSG00000211695	chromatin interactions
ENSG00000211696	chromatin interactions
ENSG00000226212	chromatin interactions
ENSG00000225992	chromatin interactions
ENSG00000231916	chromatin interactions
ENSG00000228668	chromatin interactions
ENSG00000211701	chromatin interactions
ENSG00000249978	chromatin interactions
RAB5A	miRNA target sites
CA13	miRNA target sites
SERTAD3	miRNA target sites

Extended variants
information (count: 2450 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2450 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374812911	chr7:38356596-38356597	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs369217866	chr7:38356605-38356606	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs562576258	chr7:38356642-38356643	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs374483576	chr7:38356668-38356669	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs372842829	chr7:38356691-38356692	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs375068860	chr7:38356694-38356695	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
7	rs142561064	chr7:38356701-38356702	Enhancers Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
8	rs561708920	chr7:38356725-38356726	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs114039215	chr7:38356730-38356731	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs376907181	chr7:38356737-38356738	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs118093377	chr7:38356738-38356739	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs375738278	chr7:38356741-38356742	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs377473508	chr7:38356744-38356745	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs535195920	chr7:38356759-38356760	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs112406770	chr7:38356781-38356782	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs533122825	chr7:38356786-38356787	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs375299876	chr7:38356809-38356810	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs368235775	chr7:38356810-38356811	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs181257332	chr7:38356815-38356816	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs111854601	chr7:38356838-38356839	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs56794613	chr7:38356849-38356850	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs199812390	chr7:38356865-38356866	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs372923357	chr7:38356866-38356867	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs568162779	chr7:38356889-38356890	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs534200636	chr7:38356911-38356912	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs374642798	chr7:38356926-38356927	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs34482025	chr7:38356943-38356944	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs397824959	chr7:38356950-38356951	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs146000511	chr7:38356966-38356967	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs570872954	chr7:38356996-38356997	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs367724084	chr7:38357023-38357024	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs60714066	chr7:38357040-38357041	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs374995446	chr7:38357047-38357048	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs139576690	chr7:38357048-38357049	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs369539545	chr7:38357067-38357068	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs556490351	chr7:38357068-38357069	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs144308673	chr7:38357069-38357070	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs11769443	chr7:38357075-38357076	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs561644414	chr7:38357076-38357077	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs369893658	chr7:38357116-38357117	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs58848448	chr7:38357120-38357121	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs541047040	chr7:38357121-38357122	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs184979802	chr7:38357147-38357148	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs368857948	chr7:38357148-38357149	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs373605177	chr7:38357164-38357165	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs11980080	chr7:38357194-38357195	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs549909939	chr7:38357235-38357236	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs569792981	chr7:38357285-38357286	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs11765884	chr7:38357323-38357324	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs548422833	chr7:38357331-38357332	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	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:1178 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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	chr7:38353000-38357000	Weak transcription	Primary B cells from cord blood	blood
9	chr7:38353000-38357200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr7:38353000-38357200	Weak transcription	Fetal Muscle Leg	muscle
11	chr7:38353000-38358000	Weak transcription	Spleen	Spleen
12	chr7:38353000-38358000	Weak transcription	HUVEC	blood vessel
13	chr7:38353000-38358200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr7:38353000-38358200	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr7:38353000-38358600	Enhancers	Primary hematopoietic stem cells	blood
16	chr7:38353000-38359000	Weak transcription	GM12878-XiMat	blood
17	chr7:38353000-38360800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
18	chr7:38353200-38356600	Weak transcription	Primary monocytes fromperipheralblood	blood
19	chr7:38353200-38356600	Weak transcription	Monocytes-CD14+_RO01746	blood
20	chr7:38353200-38357400	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:38353200-38357400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr7:38353200-38357600	Weak transcription	Adipose Nuclei	Adipose
23	chr7:38353200-38358200	Weak transcription	Primary T helper cells PMA-I stimulated	--
24	chr7:38353200-38358600	Weak transcription	Primary T cells from cord blood	blood
25	chr7:38353600-38357400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr7:38353600-38360800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr7:38354800-38358400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr7:38355600-38358600	Enhancers	Placenta	Placenta
29	chr7:38355600-38358800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr7:38355800-38356600	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr7:38355800-38359000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr7:38356200-38357200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
33	chr7:38356200-38357600	Weak transcription	Fetal Stomach	stomach
34	chr7:38356400-38356800	Active TSS	Fetal Thymus	thymus
35	chr7:38356400-38357800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:38356600-38356800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr7:38356600-38356800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr7:38356600-38357200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr7:38356600-38357400	Active TSS	Thymus	Thymus
40	chr7:38356600-38357800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr7:38356600-38358200	Active TSS	Primary T cells fromperipheralblood	blood
42	chr7:38356600-38358800	Enhancers	Primary monocytes fromperipheralblood	blood
43	chr7:38356800-38357200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr7:38356800-38357800	Flanking Active TSS	Fetal Thymus	thymus
45	chr7:38357000-38358000	Weak transcription	HUES48 Cell Line	embryonic stem cell
46	chr7:38357000-38358400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr7:38357000-38359200	Enhancers	Primary B cells from cord blood	blood
48	chr7:38357200-38357600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr7:38357200-38357600	Active TSS	Primary T helper naive cells from peripheral blood	blood
50	chr7:38357200-38357600	Enhancers	Duodenum Mucosa	Duodenum

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