Variant report

Variant	nsv605999
Chromosome Location	chr7:6396719-6472881
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2500)
CpG islands
(count:2321)
Chromatin interactive
region (count:103)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2500 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6432227-6433385	K562	blood:	n/a	n/a
2	ARID3A	chr7:6403396-6403567	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:6413730-6413956	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:6413828-6414114	K562	blood:	n/a	n/a
5	ARID3A	chr7:6416501-6416845	HepG2	liver:	n/a	n/a
6	ARID3A	chr7:6424825-6425475	HepG2	liver:	n/a	n/a
7	ATF1	chr7:6432902-6433406	K562	blood:	n/a	n/a
8	ATF1	chr7:6425094-6425398	K562	blood:	n/a	n/a
9	ATF1	chr7:6469907-6470154	K562	blood:	n/a	n/a
10	ATF2	chr7:6413747-6414139	GM12878	blood:	n/a	n/a
11	ATF2	chr7:6413103-6413408	GM12878	blood:	n/a	n/a
12	ATF2	chr7:6425006-6425405	GM12878	blood:	n/a	n/a
13	ATF3	chr7:6424925-6425559	HCT-116	colon:	n/a	n/a
14	ATF3	chr7:6424850-6425553	HCT-116	colon:	n/a	n/a
15	ATF3	chr7:6398701-6398975	K562	blood:	n/a	n/a
16	ATF3	chr7:6424947-6425510	A549	lung:	n/a	n/a
17	BACH1	chr7:6422631-6422760	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr7:6425804-6426093	H1-hESC	embryonic stem cell:	n/a	n/a
19	BATF	chr7:6413135-6413413	GM12878	blood:	n/a	n/a
20	BATF	chr7:6466755-6466947	GM12878	blood:	n/a	n/a
21	BATF	chr7:6413079-6413418	GM12878	blood:	n/a	n/a
22	BATF	chr7:6432890-6433246	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:6413131-6413452	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:6413154-6413328	GM12878	blood:	n/a	n/a
25	BCL3	chr7:6443320-6444094	K562	blood:	n/a	n/a
26	BCL3	chr7:6456237-6456719	A549	lung:	n/a	n/a
27	BCLAF1	chr7:6432751-6433409	GM12878	blood:	n/a	n/a
28	BCLAF1	chr7:6413747-6414199	K562	blood:	n/a	chr7:6413984-6413997 chr7:6413985-6413998
29	BCLAF1	chr7:6413837-6414196	GM12878	blood:	n/a	chr7:6413984-6413997 chr7:6413985-6413998
30	BCLAF1	chr7:6414273-6414765	GM12878	blood:	n/a	chr7:6414443-6414452 chr7:6414679-6414692 chr7:6414683-6414696 chr7:6414409-6414422 chr7:6414430-6414443
31	BDP1	chr7:6413731-6414071	Hela-S3	cervix:	n/a	n/a
32	BDP1	chr7:6413714-6414088	K562	blood:	n/a	n/a
33	BHLHE40	chr7:6413572-6414822	GM12878	blood:	n/a	chr7:6414483-6414499 chr7:6413976-6413992 chr7:6413982-6413998
34	BHLHE40	chr7:6431973-6431992	GM12878	blood:	n/a	n/a
35	BHLHE40	chr7:6413718-6414098	K562	blood:	n/a	chr7:6413976-6413992 chr7:6413982-6413998
36	BHLHE40	chr7:6413904-6414162	HepG2	liver:	n/a	chr7:6413976-6413992 chr7:6413982-6413998
37	BHLHE40	chr7:6469812-6470237	K562	blood:	n/a	n/a
38	BHLHE40	chr7:6432409-6433600	K562	blood:	n/a	n/a
39	BHLHE40	chr7:6446187-6446247	K562	blood:	n/a	n/a
40	BHLHE40	chr7:6413187-6413315	GM12878	blood:	n/a	n/a
41	BHLHE40	chr7:6414445-6414717	K562	blood:	n/a	chr7:6414483-6414499
42	BHLHE40	chr7:6432906-6433285	GM12878	blood:	n/a	n/a
43	BHLHE40	chr7:6415592-6415603	GM12878	blood:	n/a	n/a
44	BHLHE40	chr7:6407253-6407453	K562	blood:	n/a	n/a
45	BHLHE40	chr7:6456318-6456332	K562	blood:	n/a	n/a
46	BHLHE40	chr7:6416680-6416739	GM12878	blood:	n/a	n/a
47	BRCA1	chr7:6414580-6414711	GM12878	blood:	n/a	n/a
48	BRCA1	chr7:6413829-6414029	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr7:6432805-6433330	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr7:6424879-6425528	Hela-S3	cervix:	n/a	n/a

(count:2321 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6441911-6441961	T-47D	breast:	n/a
2	chr7:6413880-6413930	Jurkat	blood:	n/a
3	chr7:6449156-6449206	AG04449	skin:	fetal
4	chr7:6441911-6441961	T-47D	breast:	n/a
5	chr7:6413880-6413930	Jurkat	blood:	n/a
6	chr7:6449156-6449206	AG04449	skin:	fetal
7	chr7:6413877-6413927	SK-N-SH	brain:	n/a
8	chr7:6465684-6465734	BE2_C	brain:	n/a
9	chr7:6410669-6410719	PrEC	prostate:	n/a
10	chr7:6440601-6440651	Jurkat	blood:	n/a
11	chr7:6460966-6461016	ovcar-3	ovarian:	n/a
12	chr7:6418440-6418490	NT2-D1	testis:	n/a
13	chr7:6449615-6449665	NHDF-neo	bronchial:	n/a
14	chr7:6414708-6414758	H1-hESC	embryonic stem cell:	embryo
15	chr7:6449981-6450031	SK-N-SH	brain:	n/a
16	chr7:6448933-6448983	ovcar-3	ovarian:	n/a
17	chr7:6414708-6414758	AG09319	gingival:	n/a
18	chr7:6461393-6461443	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:6415217-6415267	ECC-1	luminal epithelium:	n/a
20	chr7:6412718-6412768	ProgFib	skin:	n/a
21	chr7:6444640-6444690	PANC-1	pancreas:	n/a
22	chr7:6418440-6418490	HCF	heart:	n/a
23	chr7:6414196-6414246	SK-N-SH_RA	brain:	n/a
24	chr7:6410669-6410719	AG04450	lung:	fetal
25	chr7:6414202-6414252	GM12891	blood:	n/a
26	chr7:6414196-6414246	Caco-2	colon:	n/a
27	chr7:6465799-6465849	RPTEC	kidney:	n/a
28	chr7:6438643-6438693	BJ	skin:	n/a
29	chr7:6438643-6438693	HEEpiC	esophagus:	n/a
30	chr7:6435978-6436028	PANC-1	pancreas:	n/a
31	chr7:6440601-6440651	HNPCEpiC	eye:	n/a
32	chr7:6442531-6442581	GM06990	blood:	n/a
33	chr7:6436101-6436151	SAEC	small airway:	n/a
34	chr7:6441514-6441564	HRE	kidney:	n/a
35	chr7:6461393-6461443	GM12892	blood:	n/a
36	chr7:6442531-6442581	HepG2	liver:	n/a
37	chr7:6442531-6442581	HRE	kidney:	n/a
38	chr7:6441514-6441564	HRCEpiC	kidney:	n/a
39	chr7:6436101-6436151	GM06990	blood:	n/a
40	chr7:6412718-6412768	MCF-7	breast:	n/a
41	chr7:6415217-6415267	GM12878	blood:	n/a
42	chr7:6449615-6449665	GM12891	blood:	n/a
43	chr7:6414708-6414758	HEEpiC	esophagus:	n/a
44	chr7:6413861-6413911	SK-N-SH_RA	brain:	n/a
45	chr7:6432590-6432640	Jurkat	blood:	n/a
46	chr7:6414708-6414758	A549	lung:	n/a
47	chr7:6444640-6444690	HMEC	breast:	n/a
48	chr7:6465684-6465734	MCF-7	breast:	n/a
49	chr7:6413877-6413927	AoSMC	blood vessel:	n/a
50	chr7:6442531-6442581	T-47D	breast:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:6410336..6412791-chr7:6523325..6524855,2	MCF-7	breast:
2	chr7:6412517..6417079-chr7:6439604..6446019,8	MCF-7	breast:
3	chr7:6425587..6427672-chr7:6434203..6435980,2	K562	blood:
4	chr7:6413088..6415412-chr7:6446957..6448818,2	MCF-7	breast:
5	chr7:6450554..6452966-chr7:6454355..6457086,3	K562	blood:
6	chr7:6390235..6392804-chr7:6397143..6398713,2	K562	blood:
7	chr7:6412448..6415033-chr7:6435116..6438429,3	MCF-7	breast:
8	chr7:6444358..6447267-chr7:6449792..6451395,2	K562	blood:
9	chr7:6459143..6461711-chr7:6462987..6466871,3	K562	blood:
10	chr7:6399153..6401648-chr7:6412367..6414838,2	K562	blood:
11	chr7:6447746..6451177-chr7:6455509..6458187,3	K562	blood:
12	chr7:6413960..6415587-chr7:6430551..6433223,4	K562	blood:
13	chr7:6412517..6417079-chr7:6439604..6446019,8	MCF-7	breast:
14	chr7:6407358..6411182-chr7:6412675..6416929,4	K562	blood:
15	chr7:6412666..6416399-chr7:6429961..6432840,4	MCF-7	breast:
16	chr7:6387187..6388731-chr7:6415190..6416736,2	K562	blood:
17	chr7:6414882..6417650-chr7:6542443..6546000,3	MCF-7	breast:
18	chr7:6413599..6415567-chr7:6443758..6446728,2	K562	blood:
19	chr7:6425039..6427961-chr7:6431283..6434070,6	K562	blood:
20	chr7:6446943..6448782-chr7:6451434..6453838,3	K562	blood:
21	chr7:6388682..6389270-chr7:6443357..6444249,2	MCF-7	breast:
22	chr7:6310725..6312409-chr7:6412991..6414709,2	K562	blood:
23	chr7:6421014..6427961-chr7:6430347..6436546,11	K562	blood:
24	chr7:6415178..6416975-chr7:6426266..6428182,2	MCF-7	breast:
25	chr7:6439401..6441053-chr7:6448696..6450255,2	K562	blood:
26	chr7:6449174..6451556-chr7:6462432..6464944,2	MCF-7	breast:
27	chr7:6424186..6426386-chr7:6428771..6430313,2	K562	blood:
28	chr7:6140966..6142574-chr7:6434049..6436038,2	K562	blood:
29	chr7:6425587..6427672-chr7:6434203..6435980,2	K562	blood:
30	chr7:6436991..6441003-chr7:6442808..6444517,3	K562	blood:
31	chr7:6463957..6465802-chr7:6468835..6470445,2	MCF-7	breast:
32	chr7:6445380..6448087-chr7:6488948..6490884,2	K562	blood:
33	chr1:43124082..43125028-chr7:6440861..6441591,2	NB4	blood:
34	chr7:6412857..6414877-chr7:6485942..6488132,2	MCF-7	breast:
35	chr7:6433852..6441003-chr7:6442415..6446485,8	K562	blood:
36	chr7:6444358..6447267-chr7:6449792..6451395,2	K562	blood:
37	chr7:6425290..6426951-chr7:6443487..6445552,2	MCF-7	breast:
38	chr7:6459143..6461711-chr7:6462987..6466871,3	K562	blood:
39	chr7:6472621..6474361-chr7:6478935..6480630,2	MCF-7	breast:
40	chr7:6413960..6415587-chr7:6430551..6433223,4	K562	blood:
41	chr7:6450208..6453839-chr7:6454159..6457397,3	MCF-7	breast:
42	chr7:6439883..6442472-chr7:6446934..6449638,2	MCF-7	breast:
43	chr7:6472532..6475025-chr7:6477721..6479595,2	MCF-7	breast:
44	chr7:6431756..6435735-chr7:6436671..6439752,6	MCF-7	breast:
45	chr7:6412666..6416399-chr7:6429961..6432840,4	MCF-7	breast:
46	chr7:6423770..6428087-chr7:6429749..6432812,3	MCF-7	breast:
47	chr14:24740456..24741347-chr7:6414145..6414731,2	Hela-S3	cervix:
48	chr7:6386938..6388709-chr7:6422840..6425617,3	MCF-7	breast:
49	chr7:6423918..6426061-chr7:6486090..6487608,2	K562	blood:
50	chr7:6413015..6417903-chr7:6435938..6439469,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAC1-1	chr7:6405329-6405671	expReg_chr7_541_+

No data

Variant related genes	Relation type
DAGLB	TF binding region
RAC1	TF binding region
DAGLB	CpG island
RAC1	CpG island
ENSG00000178397	chromatin interactions
ENSG00000008256	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000100949	chromatin interactions
ENSG00000253848	chromatin interactions
ENSG00000183808	chromatin interactions
ENSG00000171960	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000167645	chromatin interactions
ENSG00000136238	chromatin interactions
ENSG00000178896	chromatin interactions

Extended variants
information (count: 4328 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:4328 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13244632	chr7:6396719-6396720	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs200373828	chr7:6396722-6396723	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs370467401	chr7:6396753-6396754	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs76390556	chr7:6396757-6396758	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs545810463	chr7:6396775-6396776	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs182375837	chr7:6396778-6396779	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs187045195	chr7:6396790-6396791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs7788220	chr7:6396834-6396835	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs543107659	chr7:6396865-6396866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs561945680	chr7:6396908-6396909	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs377448049	chr7:6396930-6396931	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs529446815	chr7:6396938-6396939	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs191815815	chr7:6396957-6396958	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560025079	chr7:6397018-6397019	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs184335803	chr7:6397027-6397028	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs369093291	chr7:6397032-6397033	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576191398	chr7:6397038-6397039	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs551795319	chr7:6397039-6397040	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs201351550	chr7:6397051-6397052	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs112598925	chr7:6397067-6397068	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs566927142	chr7:6397098-6397099	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570065818	chr7:6397120-6397121	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs7805985	chr7:6397141-6397142	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs7805986	chr7:6397144-6397145	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs568278128	chr7:6397179-6397180	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs557524952	chr7:6397207-6397208	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs188620755	chr7:6397209-6397210	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs192968921	chr7:6397231-6397232	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539341789	chr7:6397256-6397257	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs557377504	chr7:6397263-6397264	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs575582717	chr7:6397265-6397266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs543121702	chr7:6397272-6397273	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185594610	chr7:6397288-6397289	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190468586	chr7:6397301-6397302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs541646328	chr7:6397309-6397310	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs559685297	chr7:6397334-6397335	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs151305125	chr7:6397350-6397351	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545670697	chr7:6397380-6397381	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs528267690	chr7:6397387-6397388	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs199717574	chr7:6397391-6397392	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs573093940	chr7:6397402-6397403	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs140590636	chr7:6397444-6397445	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs368737661	chr7:6397446-6397447	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs555778507	chr7:6397448-6397449	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs111560853	chr7:6397466-6397467	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs376251948	chr7:6397470-6397471	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs567773316	chr7:6397471-6397472	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs116486846	chr7:6397481-6397482	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs547609638	chr7:6397484-6397485	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs561981634	chr7:6397497-6397498	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ependymoma	20639864	CNVD
Autism	20685689	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Ovarian cancer	21781307	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:3516 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6388800-6409400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:6389000-6401800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr7:6394200-6400200	Weak transcription	HepG2	liver
4	chr7:6395400-6397000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr7:6397000-6398000	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr7:6397400-6398200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr7:6398000-6398800	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr7:6398000-6401400	Enhancers	Monocytes-CD14+_RO01746	blood
9	chr7:6398400-6399400	Enhancers	K562	blood
10	chr7:6398800-6400600	Weak transcription	Primary neutrophils fromperipheralblood	blood
11	chr7:6399200-6399600	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr7:6399400-6400400	Weak transcription	K562	blood
13	chr7:6399600-6400800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr7:6400200-6401000	Enhancers	HepG2	liver
15	chr7:6400400-6400800	Enhancers	K562	blood
16	chr7:6400600-6401000	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr7:6400600-6401000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr7:6400600-6401000	Enhancers	GM12878-XiMat	blood
19	chr7:6400800-6401200	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr7:6400800-6406800	Weak transcription	K562	blood
21	chr7:6401000-6403000	Weak transcription	HepG2	liver
22	chr7:6401400-6407200	Weak transcription	Monocytes-CD14+_RO01746	blood
23	chr7:6401800-6407000	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr7:6402400-6402600	Enhancers	Rectal Mucosa Donor 31	rectum
25	chr7:6402400-6404400	Enhancers	Fetal Intestine Large	intestine
26	chr7:6402400-6404400	Enhancers	Fetal Intestine Small	intestine
27	chr7:6402600-6403600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr7:6403000-6403600	Enhancers	HepG2	liver
29	chr7:6403600-6403800	Bivalent Enhancer	HepG2	liver
30	chr7:6403600-6404000	Enhancers	Duodenum Mucosa	Duodenum
31	chr7:6403600-6404400	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr7:6403800-6404000	Enhancers	Colonic Mucosa	Colon
33	chr7:6403800-6404200	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr7:6404000-6406400	Weak transcription	Colonic Mucosa	Colon
35	chr7:6404000-6406400	Weak transcription	Duodenum Mucosa	Duodenum
36	chr7:6404200-6406800	Weak transcription	Rectal Mucosa Donor 29	rectum
37	chr7:6404400-6406400	Weak transcription	Fetal Intestine Large	intestine
38	chr7:6404400-6406400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr7:6404400-6406800	Weak transcription	Fetal Intestine Small	intestine
40	chr7:6405600-6405800	Enhancers	Sigmoid Colon	Sigmoid Colon
41	chr7:6405800-6407400	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr7:6406400-6408000	Enhancers	Duodenum Mucosa	Duodenum
43	chr7:6406400-6408200	Enhancers	Colonic Mucosa	Colon
44	chr7:6406400-6408200	Enhancers	Fetal Intestine Large	intestine
45	chr7:6406400-6408200	Enhancers	Rectal Mucosa Donor 31	rectum
46	chr7:6406800-6407200	Enhancers	K562	blood
47	chr7:6406800-6407400	Enhancers	Hela-S3	cervix
48	chr7:6406800-6408200	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr7:6406800-6408400	Enhancers	Fetal Intestine Small	intestine
50	chr7:6407000-6408200	Enhancers	Primary monocytes fromperipheralblood	blood

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