Variant report

Variant	nsv966738
Chromosome Location	chr7:128325654-128339129
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:244)
Chromatin interactive
region (count:19)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 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	ARID3A	chr7:128337434-128338024	K562	blood:	n/a	n/a
2	ATF2	chr7:128337313-128337852	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr7:128337277-128337937	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF3	chr7:128337219-128337623	K562	blood:	n/a	n/a
5	ATF3	chr7:128337299-128337872	A549	lung:	n/a	n/a
6	ATF3	chr7:128337270-128337764	K562	blood:	n/a	n/a
7	ATF3	chr7:128337329-128337768	A549	lung:	n/a	n/a
8	BACH1	chr7:128332880-128332955	K562	blood:	n/a	n/a
9	BHLHE40	chr7:128337233-128337916	K562	blood:	n/a	n/a
10	BHLHE40	chr7:128337453-128337516	GM12878	blood:	n/a	n/a
11	BRCA1	chr7:128337474-128337928	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr7:128333727-128334129	K562	blood:	n/a	n/a
13	CBX3	chr7:128337372-128338010	K562	blood:	n/a	n/a
14	CBX3	chr7:128337197-128337990	K562	blood:	n/a	n/a
15	CCNT2	chr7:128337328-128337670	K562	blood:	n/a	n/a
16	CEBPB	chr7:128337368-128337851	K562	blood:	n/a	n/a
17	CEBPB	chr7:128337259-128337720	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr7:128331871-128332081	K562	blood:	n/a	n/a
19	CEBPB	chr7:128337321-128337524	IMR90	lung:	n/a	n/a
20	CEBPB	chr7:128337312-128338073	K562	blood:	n/a	n/a
21	CHD2	chr7:128337354-128337980	K562	blood:	n/a	n/a
22	CHD2	chr7:128337407-128337978	H1-hESC	embryonic stem cell:	n/a	n/a
23	CREB1	chr7:128337312-128337959	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr7:128337062-128338033	K562	blood:	n/a	n/a
25	CREB1	chr7:128337221-128337967	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr7:128337207-128337748	A549	lung:	n/a	n/a
27	CTCF	chr7:128337800-128337950	AG10803	skin:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
28	CTCF	chr7:128337673-128337986	GM12878	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856 chr7:128337710-128337719
29	CTCF	chr7:128337760-128337910	GM12875	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
30	CTCF	chr7:128337700-128337850	GM12864	blood:	n/a	chr7:128337710-128337719
31	CTCF	chr7:128332746-128332839	GM20000	blood:	n/a	n/a
32	CTCF	chr7:128337780-128337930	GM12868	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
33	CTCF	chr7:128337822-128337877	GM10248	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
34	CTCF	chr7:128337704-128338019	A549	lung:	n/a	chr7:128337843-128337856 chr7:128337847-128337856 chr7:128337710-128337719
35	CTCF	chr7:128337760-128337910	GM12872	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
36	CTCF	chr7:128337700-128337850	RPTEC	kidney:	n/a	chr7:128337710-128337719
37	CTCF	chr7:128337800-128337950	HFF	foreskin:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
38	CTCF	chr7:128337710-128337942	SK-N-SH_RA	brain:	n/a	chr7:128337843-128337856 chr7:128337847-128337856 chr7:128337710-128337719
39	CTCF	chr7:128337790-128337929	HUVEC	blood vessel:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
40	CTCF	chr7:128337820-128337970	GM12869	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
41	CTCF	chr7:128337800-128337950	GM12873	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
42	CTCF	chr7:128337800-128337950	BJ	skin:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
43	CTCF	chr7:128337786-128337926	GM10266	blood:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
44	CTCF	chr7:128337800-128337950	HBMEC	blood vessel:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
45	CTCF	chr7:128337800-128337950	HCFaa	heart:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
46	CTCF	chr7:128337800-128337950	HMF	breast:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
47	CTCF	chr7:128337780-128337930	HFF-Myc	foreskin:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
48	CTCF	chr7:128337620-128337770	NHDF-neo	bronchial:	n/a	chr7:128337710-128337719
49	CTCF	chr7:128337724-128337953	H1-hESC	embryonic stem cell:	n/a	chr7:128337843-128337856 chr7:128337847-128337856
50	CTCF	chr7:128337480-128337630	GM12872	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128337621-128337671	U87	brain:	n/a
2	chr7:128338932-128338982	ProgFib	skin:	n/a
3	chr7:128338932-128338982	HPAEpiC	pulmonary alveolar:	n/a
4	chr7:128337483-128337533	SKMC	muscle:	n/a
5	chr7:128337483-128337533	SK-N-MC	brain:	n/a
6	chr7:128337483-128337533	HCT-116	colon:	n/a
7	chr7:128337725-128337775	ovcar-3	ovarian:	n/a
8	chr7:128337725-128337775	HL-60	blood:	n/a
9	chr7:128338932-128338982	BJ	skin:	n/a
10	chr7:128337621-128337671	NB4	blood:	n/a
11	chr7:128338932-128338982	ECC-1	luminal epithelium:	n/a
12	chr7:128337621-128337671	Hepatocyte	liver:	n/a
13	chr7:128338932-128338982	HCM	heart:	n/a
14	chr7:128338932-128338982	CMK	blood:	n/a
15	chr7:128337483-128337533	AG04449	skin:	fetal
16	chr7:128337725-128337775	NT2-D1	testis:	n/a
17	chr7:128337621-128337671	ovcar-3	ovarian:	n/a
18	chr7:128338932-128338982	SK-N-SH	brain:	n/a
19	chr7:128337725-128337775	CMK	blood:	n/a
20	chr7:128338932-128338982	K562	blood:	n/a
21	chr7:128338932-128338982	MCF-7	breast:	n/a
22	chr7:128337725-128337775	AG04449	skin:	fetal
23	chr7:128337621-128337671	NH-A	brain:	n/a
24	chr7:128337483-128337533	NT2-D1	testis:	n/a
25	chr7:128337621-128337671	BJ	skin:	n/a
26	chr7:128337621-128337671	Caco-2	colon:	n/a
27	chr7:128337621-128337671	HCT-116	colon:	n/a
28	chr7:128337725-128337775	HepG2	liver:	n/a
29	chr7:128337483-128337533	GM12891	blood:	n/a
30	chr7:128337725-128337775	PANC-1	pancreas:	n/a
31	chr7:128337621-128337671	AG09319	gingival:	n/a
32	chr7:128337621-128337671	Hela-S3	cervix:	n/a
33	chr7:128337621-128337671	A549	lung:	n/a
34	chr7:128337483-128337533	HMEC	breast:	n/a
35	chr7:128337621-128337671	GM19239	blood:	n/a
36	chr7:128337483-128337533	NH-A	brain:	n/a
37	chr7:128338932-128338982	AG10803	skin:	n/a
38	chr7:128337725-128337775	GM12892	blood:	n/a
39	chr7:128337725-128337775	AG04450	lung:	fetal
40	chr7:128337483-128337533	Hepatocyte	liver:	n/a
41	chr7:128337725-128337775	NB4	blood:	n/a
42	chr7:128337621-128337671	HIPEpiC	eye:	n/a
43	chr7:128337483-128337533	AG09309	skin:	n/a
44	chr7:128338932-128338982	HCT-116	colon:	n/a
45	chr7:128337483-128337533	AoSMC	blood vessel:	n/a
46	chr7:128337725-128337775	AG09309	skin:	n/a
47	chr7:128337725-128337775	BE2_C	brain:	n/a
48	chr7:128338932-128338982	GM12891	blood:	n/a
49	chr7:128337483-128337533	HPAEpiC	pulmonary alveolar:	n/a
50	chr7:128337621-128337671	AoSMC	blood vessel:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:128331712..128335200-chr7:128335875..128338019,5	K562	blood:
2	chr7:128311765..128313824-chr7:128325788..128328720,2	K562	blood:
3	chr7:128171099..128172769-chr7:128337309..128338976,2	K562	blood:
4	chr7:128332579..128336216-chr7:128338226..128341696,3	K562	blood:
5	chr7:128331833..128334672-chr7:128377724..128379634,3	K562	blood:
6	chr7:128335950..128337801-chr7:128377957..128380302,2	K562	blood:
7	chr7:128320147..128324613-chr7:128325598..128330219,5	K562	blood:
8	chr7:128311065..128312727-chr7:128337751..128339462,2	K562	blood:
9	chr7:128331712..128335200-chr7:128335875..128338019,5	K562	blood:
10	chr7:128331101..128332933-chr7:128334732..128337486,2	MCF-7	breast:
11	chr7:128049553..128051541-chr7:128337995..128340649,2	K562	blood:
12	chr7:128335938..128338927-chr7:128468938..128472224,3	K562	blood:
13	chr7:128335075..128336682-chr7:128523821..128526659,2	K562	blood:
14	chr7:128331101..128332933-chr7:128334732..128337486,2	MCF-7	breast:
15	chr7:128334725..128337091-chr7:128364538..128366706,2	K562	blood:
16	chr7:128325647..128328540-chr7:128329512..128331138,2	MCF-7	breast:
17	chr7:128325647..128328540-chr7:128329512..128331138,2	MCF-7	breast:
18	chr7:128330435..128332663-chr7:128334288..128336235,2	K562	blood:
19	chr7:128337259..128338313-chr7:128519735..128520778,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71F2-3	chr7:128327342-128327926	ENSG00000270810.1
2	lnc-FAM71F2-6	chr7:128333504-128333978	NONHSAT123245
3	lnc-FAM71F2-4	chr7:128330505-128331771	ENSG00000271344.1

No data

Variant related genes	Relation type
IMP3P2	TF binding region
ENSG00000270810	TF binding region
RNA5SP242	TF binding region
RNA5SP243	TF binding region
ENSG00000271344	TF binding region
IMP3P2	CpG island
ENSG00000270810	CpG island
RNA5SP242	CpG island
RNA5SP243	CpG island
ENSG00000271344	CpG island
ENSG00000271344	chromatin interactions
ENSG00000128591	chromatin interactions
ENSG00000242588	chromatin interactions
ENSG00000106348	chromatin interactions
ENSG00000128595	chromatin interactions
ENSG00000239722	chromatin interactions
ENSG00000273270	chromatin interactions
ENSG00000205085	chromatin interactions
ENSG00000201041	chromatin interactions
ENSG00000270810	chromatin interactions
ENSG00000135253	chromatin interactions
ENSG00000252866	chromatin interactions

Extended variants
information (count: 501 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577274368	chr7:128325761-128325762	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs541204384	chr7:128325820-128325821	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs75228562	chr7:128325841-128325842	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs574519257	chr7:128325899-128325900	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs118135504	chr7:128325908-128325909	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs147468349	chr7:128325922-128325923	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531473343	chr7:128325947-128325948	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs112658130	chr7:128325957-128325958	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs549950911	chr7:128325975-128325976	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs564890198	chr7:128325984-128325985	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs532324739	chr7:128326007-128326008	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs375706856	chr7:128326016-128326017	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs547223791	chr7:128326030-128326031	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs565760531	chr7:128326038-128326039	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs139976376	chr7:128326050-128326051	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs548175383	chr7:128326051-128326052	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs570388282	chr7:128326072-128326073	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs537302147	chr7:128326136-128326137	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs559191058	chr7:128326150-128326151	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145483252	chr7:128326160-128326161	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs535196753	chr7:128326224-128326225	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs557180420	chr7:128326229-128326230	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs553082490	chr7:128326230-128326231	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs201665320	chr7:128326260-128326261	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs368845385	chr7:128326261-128326262	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs184331744	chr7:128326262-128326263	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs377249363	chr7:128326267-128326268	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs189611127	chr7:128326270-128326271	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs566388409	chr7:128326314-128326315	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs576400595	chr7:128326373-128326374	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs78567332	chr7:128326403-128326404	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs11982488	chr7:128326432-128326433	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs575939622	chr7:128326457-128326458	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113609660	chr7:128326477-128326478	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs543392983	chr7:128326522-128326523	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562070015	chr7:128326554-128326555	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs181212324	chr7:128326561-128326562	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs532236386	chr7:128326633-128326634	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs147605058	chr7:128326637-128326638	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs559507719	chr7:128326669-128326670	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs529788777	chr7:128326747-128326748	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs548213565	chr7:128326789-128326790	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs569632585	chr7:128326793-128326794	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs527772017	chr7:128326812-128326813	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs185798266	chr7:128326817-128326818	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs149732940	chr7:128326822-128326823	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs199686248	chr7:128326825-128326826	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs534920647	chr7:128326854-128326855	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs188946606	chr7:128326869-128326870	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs568217331	chr7:128326876-128326877	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Melanoma	20877625	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:392 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128294800-128328000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:128298600-128329200	Weak transcription	Pancreas	Pancrea
3	chr7:128302400-128337200	Weak transcription	Gastric	stomach
4	chr7:128302600-128327800	Weak transcription	Placenta	Placenta
5	chr7:128310000-128329400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr7:128311200-128327000	Weak transcription	HSMM	muscle
7	chr7:128311600-128327800	Weak transcription	Brain Substantia Nigra	brain
8	chr7:128313400-128329400	Weak transcription	Esophagus	oesophagus
9	chr7:128313400-128331200	Weak transcription	Stomach Smooth Muscle	stomach
10	chr7:128313600-128327200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr7:128313600-128327600	Weak transcription	Duodenum Smooth Muscle	Duodenum
12	chr7:128313600-128337200	Weak transcription	Right Atrium	heart
13	chr7:128318200-128327600	Weak transcription	NHEK	skin
14	chr7:128318200-128328000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:128318400-128325800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:128319400-128328000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr7:128319800-128328000	Weak transcription	Fetal Intestine Small	intestine
18	chr7:128320200-128332000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:128320200-128337200	Weak transcription	NHLF	lung
20	chr7:128320400-128331000	Weak transcription	Brain Angular Gyrus	brain
21	chr7:128320400-128331000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chr7:128320800-128329400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr7:128321000-128332000	Weak transcription	Fetal Brain Male	brain
24	chr7:128321800-128328000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr7:128322000-128325800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr7:128322000-128328000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
27	chr7:128322200-128328800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr7:128322200-128333000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr7:128322400-128326000	Strong transcription	Skeletal Muscle Female	skeletal muscle
30	chr7:128322600-128326400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr7:128322600-128328800	Weak transcription	Brain Germinal Matrix	brain
32	chr7:128323000-128326600	Strong transcription	Adipose Nuclei	Adipose
33	chr7:128323400-128326400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr7:128323400-128326400	Weak transcription	NH-A	brain
35	chr7:128323400-128327000	Weak transcription	NHDF-Ad	bronchial
36	chr7:128323400-128327600	Weak transcription	HSMMtube	muscle
37	chr7:128323400-128337200	Weak transcription	Left Ventricle	heart
38	chr7:128324000-128326800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr7:128324200-128337200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr7:128324400-128326200	Weak transcription	Fetal Brain Female	brain
41	chr7:128324400-128330200	Weak transcription	Fetal Muscle Leg	muscle
42	chr7:128324400-128330600	Weak transcription	Osteobl	bone
43	chr7:128324400-128337200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr7:128324600-128330800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:128324800-128330800	Weak transcription	Fetal Muscle Trunk	muscle
46	chr7:128325200-128325800	Strong transcription	Ovary	ovary
47	chr7:128325200-128326000	Strong transcription	Brain Hippocampus Middle	brain
48	chr7:128325400-128325800	Strong transcription	Aorta	Aorta
49	chr7:128325400-128326000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr7:128325600-128326000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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