Variant report

Variant	nsv518432
Chromosome Location	chr7:100056166-100064719
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:327)
CpG islands
(count:427)
Chromatin interactive
region (count:18)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:327 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr7:100063364-100063727	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr7:100063233-100063655	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr7:100063607-100063640	K562	blood:	n/a	n/a
4	BRCA1	chr7:100063526-100063650	HepG2	liver:	n/a	n/a
5	CBX3	chr7:100063325-100063790	K562	blood:	n/a	n/a
6	CCNT2	chr7:100063600-100063839	K562	blood:	n/a	chr7:100063818-100063827
7	CHD2	chr7:100063445-100063611	H1-hESC	embryonic stem cell:	n/a	n/a
8	CREB1	chr7:100063436-100063822	A549	lung:	n/a	n/a
9	CTCF	chr7:100063540-100063690	HCFaa	heart:	n/a	chr7:100063605-100063613
10	CTCF	chr7:100063520-100063670	HFF	foreskin:	n/a	chr7:100063605-100063613
11	CTCF	chr7:100063506-100063733	Medullo	brain:	n/a	chr7:100063605-100063613
12	CTCF	chr7:100063549-100063688	MCF-7	breast:	n/a	chr7:100063605-100063613
13	CTCF	chr7:100063498-100063729	MCF-7	breast:	n/a	chr7:100063605-100063613
14	CTCF	chr7:100063520-100063670	HepG2	liver:	n/a	chr7:100063605-100063613
15	CTCF	chr7:100063540-100063690	HMEC	breast:	n/a	chr7:100063605-100063613
16	CTCF	chr7:100063523-100063721	Kidney_OC	kidney:	n/a	chr7:100063605-100063613
17	CTCF	chr7:100063560-100063710	HFF-Myc	foreskin:	n/a	chr7:100063605-100063613
18	CTCF	chr7:100063565-100063664	GM10266	blood:	n/a	chr7:100063605-100063613
19	CTCF	chr7:100063535-100063703	GM12878	blood:	n/a	chr7:100063605-100063613
20	CTCF	chr7:100063520-100063670	HRE	kidney:	n/a	chr7:100063605-100063613
21	CTCF	chr7:100063520-100063670	RPTEC	kidney:	n/a	chr7:100063605-100063613
22	CTCF	chr7:100063502-100063720	NHEK	skin:	n/a	chr7:100063605-100063613
23	CTCF	chr7:100063540-100063690	HEK293	kidney:	n/a	chr7:100063605-100063613
24	CTCF	chr7:100063500-100063650	GM12866	blood:	n/a	chr7:100063605-100063613
25	CTCF	chr7:100063520-100063670	HMF	breast:	n/a	chr7:100063605-100063613
26	CTCF	chr7:100063440-100063590	GM12865	blood:	n/a	n/a
27	CTCF	chr7:100063560-100063710	NHEK	skin:	n/a	chr7:100063605-100063613
28	CTCF	chr7:100062881-100063965	SK-N-SH	brain:	n/a	chr7:100063605-100063613
29	CTCF	chr7:100063584-100063644	GM10248	blood:	n/a	chr7:100063605-100063613
30	CTCF	chr7:100063524-100063702	MCF-7	breast:	n/a	chr7:100063605-100063613
31	CTCF	chr7:100063520-100063670	HCPEpiC	choroid plexus:	n/a	chr7:100063605-100063613
32	CTCF	chr7:100063560-100063710	HPAF	blood vessel:	n/a	chr7:100063605-100063613
33	CTCF	chr7:100063560-100063710	BJ	skin:	n/a	chr7:100063605-100063613
34	CTCF	chr7:100063386-100063716	K562	blood:	n/a	chr7:100063605-100063613
35	CTCF	chr7:100063440-100063590	HAc	cerebellar:	n/a	n/a
36	CTCF	chr7:100063520-100063670	GM12873	blood:	n/a	chr7:100063605-100063613
37	CTCF	chr7:100063520-100063670	WI-38	lung:	n/a	chr7:100063605-100063613
38	CTCF	chr7:100063560-100063710	HVMF	connective:	n/a	chr7:100063605-100063613
39	CTCF	chr7:100063357-100063945	HCT-116	colon:	n/a	chr7:100063605-100063613
40	CTCF	chr7:100063500-100063650	GM12874	blood:	n/a	chr7:100063605-100063613
41	CTCF	chr7:100063461-100063716	HUVEC	blood vessel:	n/a	chr7:100063605-100063613
42	CTCF	chr7:100063520-100063670	HEEpiC	esophagus:	n/a	chr7:100063605-100063613
43	CTCF	chr7:100063473-100063743	K562	blood:	n/a	chr7:100063605-100063613
44	CTCF	chr7:100063500-100063650	HA-sp	spinal cord:	n/a	chr7:100063605-100063613
45	CTCF	chr7:100063460-100063741	SK-N-SH_RA	brain:	n/a	chr7:100063605-100063613
46	CTCF	chr7:100063506-100063695	GM19240	blood:	n/a	chr7:100063605-100063613
47	CTCF	chr7:100063520-100063670	HCT-116	colon:	n/a	chr7:100063605-100063613
48	CTCF	chr7:100063356-100063724	H1-hESC	embryonic stem cell:	n/a	chr7:100063605-100063613
49	CTCF	chr7:100063500-100063650	AG04450	lung:	n/a	chr7:100063605-100063613
50	CTCF	chr7:100063505-100063714	MCF-7	breast:	n/a	chr7:100063605-100063613

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:100064671-100064721	GM12891	blood:	n/a
2	chr7:100062030-100062080	ECC-1	luminal epithelium:	n/a
3	chr7:100061611-100061661	HL-60	blood:	n/a
4	chr7:100064619-100064669	A549	lung:	n/a
5	chr7:100064485-100064535	GM12892	blood:	n/a
6	chr7:100064485-100064535	AG04450	lung:	fetal
7	chr7:100063101-100063151	SK-N-SH_RA	brain:	n/a
8	chr7:100062030-100062080	GM19239	blood:	n/a
9	chr7:100063101-100063151	K562	blood:	n/a
10	chr7:100064671-100064721	HMEC	breast:	n/a
11	chr7:100064619-100064669	HEK293	kidney:	embryo
12	chr7:100064671-100064721	SKMC	muscle:	n/a
13	chr7:100062821-100062871	HRE	kidney:	n/a
14	chr7:100062030-100062080	ProgFib	skin:	n/a
15	chr7:100063101-100063151	IMR90	lung:	fetal
16	chr7:100063101-100063151	HCF	heart:	n/a
17	chr7:100062030-100062080	AG10803	skin:	n/a
18	chr7:100064671-100064721	SK-N-SH_RA	brain:	n/a
19	chr7:100062821-100062871	HRPEpiC	eye:	n/a
20	chr7:100064485-100064535	GM19239	blood:	n/a
21	chr7:100062821-100062871	HEEpiC	esophagus:	n/a
22	chr7:100064485-100064535	Hela-S3	cervix:	n/a
23	chr7:100062030-100062080	HMEC	breast:	n/a
24	chr7:100064485-100064535	HNPCEpiC	eye:	n/a
25	chr7:100062821-100062871	PFSK-1	brain:	n/a
26	chr7:100062821-100062871	SAEC	small airway:	n/a
27	chr7:100062821-100062871	A549	lung:	n/a
28	chr7:100064671-100064721	HEEpiC	esophagus:	n/a
29	chr7:100061611-100061661	AG10803	skin:	n/a
30	chr7:100062821-100062871	NB4	blood:	n/a
31	chr7:100063101-100063151	Hela-S3	cervix:	n/a
32	chr7:100064485-100064535	ovcar-3	ovarian:	n/a
33	chr7:100062030-100062080	HCF	heart:	n/a
34	chr7:100064619-100064669	NHBE	bronchial:	n/a
35	chr7:100063101-100063151	PFSK-1	brain:	n/a
36	chr7:100062821-100062871	Hepatocyte	liver:	n/a
37	chr7:100064485-100064535	HCM	heart:	n/a
38	chr7:100061611-100061661	SK-N-SH_RA	brain:	n/a
39	chr7:100062821-100062871	RPTEC	kidney:	n/a
40	chr7:100064485-100064535	HMEC	breast:	n/a
41	chr7:100064619-100064669	U87	brain:	n/a
42	chr7:100063101-100063151	GM19239	blood:	n/a
43	chr7:100063101-100063151	ovcar-3	ovarian:	n/a
44	chr7:100064671-100064721	Hela-S3	cervix:	n/a
45	chr7:100061611-100061661	NHDF-neo	bronchial:	n/a
46	chr7:100061611-100061661	U87	brain:	n/a
47	chr7:100064619-100064669	GM19239	blood:	n/a
48	chr7:100064485-100064535	NH-A	brain:	n/a
49	chr7:100064671-100064721	HCM	heart:	n/a
50	chr7:100062030-100062080	MCF-7	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:100054484..100057296-chr7:100067069..100069392,2	K562	blood:
2	chr7:100063244..100066111-chr7:100151596..100153457,2	K562	blood:
3	chr7:100063127..100064075-chr7:100157483..100158054,3	MCF-7	breast:
4	chr7:100031120..100032907-chr7:100059800..100061803,2	K562	blood:
5	chr7:100057222..100060503-chr7:100060567..100064280,4	K562	blood:
6	chr7:100063136..100063863-chr7:100080545..100081488,4	K562	blood:
7	chr7:100059236..100061028-chr7:100176403..100178856,2	K562	blood:
8	chr7:100054541..100057422-chr7:100065682..100067622,2	K562	blood:
9	chr7:100025305..100026839-chr7:100054628..100057222,2	MCF-7	breast:
10	chr7:100027421..100030245-chr7:100062292..100064622,2	MCF-7	breast:
11	chr7:100063079..100063989-chr7:100144215..100144855,2	K562	blood:
12	chr7:100025026..100028437-chr7:100054589..100058212,3	K562	blood:
13	chr7:100025648..100028089-chr7:100060408..100062284,2	K562	blood:
14	chr7:100024644..100031194-chr7:100062394..100068680,9	K562	blood:
15	chr7:100033593..100036077-chr7:100064067..100067059,3	K562	blood:
16	chr7:100057222..100060503-chr7:100060567..100064280,4	K562	blood:
17	chr7:100063964..100066067-chr7:100271416..100274399,2	K562	blood:
18	chr7:100025212..100026882-chr7:100058057..100059970,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NYAP1-5	chr7:100060452-100060725	NONHSAT122377

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	TSC22D4	hsa-miR-124-3p	chr7:100064561-100064555

Variant related genes	Relation type
RN7SL161P	TF binding region
C7orf61	TF binding region
RN7SL161P	CpG island
C7orf61	CpG island
ENSG00000077454	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000240211	chromatin interactions
ENSG00000106351	chromatin interactions
ENSG00000185955	chromatin interactions
ENSG00000172354	chromatin interactions
ENSG00000241357	chromatin interactions
ENSG00000266372	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000264758	chromatin interactions
ENSG00000160813	chromatin interactions
ENSG00000166925	chromatin interactions

Extended variants
information (count: 325 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:325 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6955362	chr7:100056166-100056167	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs550547372	chr7:100056170-100056171	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs568603810	chr7:100056197-100056198	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs532897971	chr7:100056205-100056206	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs6975514	chr7:100056220-100056221	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs147283001	chr7:100056231-100056232	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs200507052	chr7:100056315-100056316	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs13228741	chr7:100056345-100056346	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs534195548	chr7:100056347-100056348	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs535544022	chr7:100056405-100056406	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs183683950	chr7:100056443-100056444	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs556036069	chr7:100056463-100056464	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs373873621	chr7:100056472-100056473	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs58276627	chr7:100056474-100056475	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs567709545	chr7:100056487-100056488	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs538423191	chr7:100056505-100056506	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs187499676	chr7:100056546-100056547	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs77659009	chr7:100056567-100056568	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs190674089	chr7:100056586-100056587	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs207468336	chr7:100056615-100056616	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs201018894	chr7:100056623-100056624	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs199513220	chr7:100056626-100056627	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs35257323	chr7:100056627-100056628	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs548712268	chr7:100056705-100056706	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs545537812	chr7:100056707-100056708	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs377268817	chr7:100056724-100056725	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs572413773	chr7:100056782-100056783	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs369460033	chr7:100056786-100056787	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs562736892	chr7:100056794-100056795	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs187110161	chr7:100056850-100056851	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs529215119	chr7:100056869-100056870	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs543988967	chr7:100056876-100056877	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs562372172	chr7:100056878-100056879	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs532836446	chr7:100056908-100056909	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs191918356	chr7:100056918-100056919	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs374097085	chr7:100056928-100056929	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs377145913	chr7:100056943-100056944	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs182686568	chr7:100056951-100056952	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs368143747	chr7:100056980-100056981	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs527286040	chr7:100057011-100057012	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs548752985	chr7:100057028-100057029	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs374977103	chr7:100057091-100057092	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs140697231	chr7:100057092-100057093	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs200071367	chr7:100057099-100057100	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs538182534	chr7:100057120-100057121	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs528287832	chr7:100057121-100057122	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs571883349	chr7:100057133-100057134	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs144644366	chr7:100057137-100057138	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs554309967	chr7:100057164-100057165	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs188206709	chr7:100057178-100057179	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:100048400-100062800	Weak transcription	Fetal Heart	heart
2	chr7:100048600-100057200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr7:100048600-100058000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr7:100048600-100058000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:100048600-100058200	Weak transcription	Primary B cells from cord blood	blood
6	chr7:100048600-100058400	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr7:100048600-100060200	Weak transcription	Brain Germinal Matrix	brain
8	chr7:100048600-100060800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:100048600-100060800	Weak transcription	NHDF-Ad	bronchial
10	chr7:100048600-100061000	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr7:100048600-100061000	Weak transcription	Esophagus	oesophagus
12	chr7:100048600-100061000	Weak transcription	HSMM	muscle
13	chr7:100048600-100061200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr7:100048600-100061200	Weak transcription	NHLF	lung
15	chr7:100048600-100063000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr7:100048600-100063200	Weak transcription	Osteobl	bone
17	chr7:100048600-100063600	Weak transcription	Ovary	ovary
18	chr7:100048600-100064200	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr7:100048600-100064400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr7:100048600-100064800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr7:100048600-100064800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr7:100048600-100068200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:100048600-100070400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr7:100048600-100070400	Weak transcription	HSMMtube	muscle
25	chr7:100048800-100058400	Weak transcription	Primary monocytes fromperipheralblood	blood
26	chr7:100048800-100058400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr7:100048800-100060600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr7:100048800-100060800	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr7:100048800-100063000	Weak transcription	Adipose Nuclei	Adipose
30	chr7:100048800-100063000	Weak transcription	Liver	Liver
31	chr7:100048800-100063000	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr7:100048800-100063000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr7:100048800-100063400	Weak transcription	Left Ventricle	heart
34	chr7:100048800-100064400	Weak transcription	Fetal Intestine Large	intestine
35	chr7:100048800-100064600	Weak transcription	Duodenum Mucosa	Duodenum
36	chr7:100048800-100064800	Weak transcription	NHEK	skin
37	chr7:100049200-100063000	Weak transcription	Pancreas	Pancrea
38	chr7:100050200-100064600	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr7:100052800-100064600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
40	chr7:100052800-100066800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr7:100053000-100058200	Weak transcription	Primary hematopoietic stem cells	blood
42	chr7:100053000-100061000	Weak transcription	HUVEC	blood vessel
43	chr7:100053000-100061200	Weak transcription	Primary T helper cells PMA-I stimulated	--
44	chr7:100053000-100063200	Weak transcription	GM12878-XiMat	blood
45	chr7:100053000-100064400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr7:100053000-100064600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
47	chr7:100053000-100064600	Weak transcription	Dnd41	blood
48	chr7:100053200-100057200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr7:100053600-100057200	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr7:100053600-100058800	Strong transcription	Brain Substantia Nigra	brain

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