Variant report

Variant	nsv1018890
Chromosome Location	chr7:38557432-38600944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:153)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:153 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:38589643-38589799	A549	lung:	n/a	chr7:38589727-38589738
2	CEBPB	chr7:38589584-38589898	HepG2	liver:	n/a	chr7:38589727-38589738
3	CEBPB	chr7:38600725-38600980	IMR90	lung:	n/a	n/a
4	CEBPB	chr7:38585579-38585804	K562	blood:	n/a	n/a
5	CEBPB	chr7:38581750-38582054	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:38589585-38589852	IMR90	lung:	n/a	chr7:38589727-38589738
7	CEBPB	chr7:38585591-38585831	MCF-7	breast:	n/a	n/a
8	CEBPB	chr7:38585213-38585302	HepG2	liver:	n/a	n/a
9	CTCF	chr7:38579720-38579870	NB4	blood:	n/a	n/a
10	CTCF	chr7:38585680-38585830	HepG2	liver:	n/a	n/a
11	CTCF	chr7:38579523-38579976	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:38585691-38585853	MCF-7	breast:	n/a	n/a
13	CTCF	chr7:38579360-38579510	AG10803	skin:	n/a	n/a
14	CTCF	chr7:38579666-38579793	GM12878	blood:	n/a	n/a
15	CTCF	chr7:38579620-38579770	AG10803	skin:	n/a	n/a
16	CTCF	chr7:38585720-38585870	NB4	blood:	n/a	n/a
17	CTCF	chr7:38579680-38579830	AG09319	gingival:	n/a	n/a
18	CTCF	chr7:38567920-38568070	HMEC	breast:	n/a	n/a
19	CTCF	chr7:38579640-38579790	AG09319	gingival:	n/a	n/a
20	CTCF	chr7:38579700-38579850	GM12864	blood:	n/a	n/a
21	CTCF	chr7:38579640-38579790	GM12873	blood:	n/a	n/a
22	CTCF	chr7:38579760-38579910	AG09309	skin:	n/a	n/a
23	CTCF	chr7:38585640-38585790	MCF-7	breast:	n/a	n/a
24	CTCF	chr7:38600920-38601070	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:38585760-38585910	HMF	breast:	n/a	n/a
26	CTCF	chr7:38585680-38585830	MCF-7	breast:	n/a	n/a
27	CTCF	chr7:38585660-38585810	GM12875	blood:	n/a	n/a
28	CTCF	chr7:38585686-38585852	K562	blood:	n/a	n/a
29	CTCF	chr7:38579700-38579850	AG10803	skin:	n/a	n/a
30	CTCF	chr7:38579700-38579850	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:38585660-38585810	A549	lung:	n/a	n/a
32	CTCF	chr7:38600920-38601070	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr7:38585717-38585840	K562	blood:	n/a	n/a
34	CTCF	chr7:38579660-38579810	GM12874	blood:	n/a	n/a
35	CTCF	chr7:38585700-38585850	GM12864	blood:	n/a	n/a
36	CTCF	chr7:38585640-38585790	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr7:38600940-38601090	AG09309	skin:	n/a	n/a
38	CTCF	chr7:38585710-38585850	MCF-7	breast:	n/a	n/a
39	CTCF	chr7:38585660-38585810	HepG2	liver:	n/a	n/a
40	CTCF	chr7:38585594-38585865	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr7:38579700-38579850	AG04449	skin:	n/a	n/a
42	CTCF	chr7:38579709-38579751	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:38579420-38579570	GM12864	blood:	n/a	n/a
44	CTCF	chr7:38579760-38579910	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:38585720-38585870	HCT-116	colon:	n/a	n/a
46	CTCF	chr7:38579700-38579850	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr7:38579702-38579833	GM12878	blood:	n/a	n/a
48	CTCF	chr7:38585700-38585850	GM12873	blood:	n/a	n/a
49	CTCF	chr7:38579660-38579810	HEK293	kidney:	n/a	n/a
50	CTCF	chr7:38579600-38579750	HPF	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:38598910-38598960	HIPEpiC	eye:	n/a
2	chr7:38598910-38598960	IMR90	lung:	fetal
3	chr7:38580353-38580403	NH-A	brain:	n/a
4	chr7:38580353-38580403	MCF-7	breast:	n/a
5	chr7:38598910-38598960	HEK293	kidney:	embryo
6	chr7:38598910-38598960	HAEpiC	amniotic membrane:	n/a
7	chr7:38580353-38580403	A549	lung:	n/a
8	chr7:38598910-38598960	HPAEpiC	pulmonary alveolar:	n/a
9	chr7:38580353-38580403	ECC-1	luminal epithelium:	n/a
10	chr7:38598910-38598960	ECC-1	luminal epithelium:	n/a
11	chr7:38598910-38598960	AoSMC	blood vessel:	n/a
12	chr7:38598910-38598960	LNCaP	prostate:	n/a
13	chr7:38598910-38598960	HRPEpiC	eye:	n/a
14	chr7:38580353-38580403	T-47D	breast:	n/a
15	chr7:38580353-38580403	SK-N-MC	brain:	n/a
16	chr7:38580353-38580403	Hela-S3	cervix:	n/a
17	chr7:38580353-38580403	HNPCEpiC	eye:	n/a
18	chr7:38580353-38580403	AG04449	skin:	fetal
19	chr7:38598910-38598960	HCPEpiC	choroid plexus:	n/a
20	chr7:38580353-38580403	HUVEC	blood vessel:	n/a
21	chr7:38598910-38598960	ovcar-3	ovarian:	n/a
22	chr7:38598910-38598960	BJ	skin:	n/a
23	chr7:38580353-38580403	BE2_C	brain:	n/a
24	chr7:38598910-38598960	GM19239	blood:	n/a
25	chr7:38580353-38580403	NHDF-neo	bronchial:	n/a
26	chr7:38580353-38580403	HRPEpiC	eye:	n/a
27	chr7:38580353-38580403	HCF	heart:	n/a
28	chr7:38598910-38598960	HRCEpiC	kidney:	n/a
29	chr7:38598910-38598960	AG10803	skin:	n/a
30	chr7:38598910-38598960	H1-hESC	embryonic stem cell:	embryo
31	chr7:38598910-38598960	PANC-1	pancreas:	n/a
32	chr7:38598910-38598960	SK-N-SH_RA	brain:	n/a
33	chr7:38598910-38598960	Hela-S3	cervix:	n/a
34	chr7:38598910-38598960	A549	lung:	n/a
35	chr7:38598910-38598960	SK-N-MC	brain:	n/a
36	chr7:38598910-38598960	NHBE	bronchial:	n/a
37	chr7:38580353-38580403	HCT-116	colon:	n/a
38	chr7:38580353-38580403	AoSMC	blood vessel:	n/a
39	chr7:38598910-38598960	GM12878	blood:	n/a
40	chr7:38580353-38580403	HRCEpiC	kidney:	n/a
41	chr7:38580353-38580403	GM12891	blood:	n/a
42	chr7:38598910-38598960	HepG2	liver:	n/a
43	chr7:38598910-38598960	NT2-D1	testis:	n/a
44	chr7:38580353-38580403	LNCaP	prostate:	n/a
45	chr7:38598910-38598960	PFSK-1	brain:	n/a
46	chr7:38580353-38580403	IMR90	lung:	fetal
47	chr7:38580353-38580403	SKMC	muscle:	n/a
48	chr7:38598910-38598960	HNPCEpiC	eye:	n/a
49	chr7:38580353-38580403	NT2-D1	testis:	n/a
50	chr7:38580353-38580403	HAEpiC	amniotic membrane:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:38557963..38559634-chr7:38569401..38571680,2	K562	blood:
2	chr7:38599177..38602352-chr7:38604364..38606813,3	K562	blood:
3	chr7:38567671..38572495-chr7:38573496..38576413,4	K562	blood:
4	chr7:38600195..38602352-chr7:38604364..38606243,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM183B-5	chr7:38570642-38570939	NONHSAT120188

No data

Variant related genes	Relation type
RN7SL83P	TF binding region
RN7SL83P	CpG island
ENSG00000241756	chromatin interactions
SESN1	miRNA target sites

Extended variants
information (count: 1537 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1537 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556784073	chr7:38557896-38557897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs542845862	chr7:38557905-38557906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs371309103	chr7:38557916-38557917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567313801	chr7:38557952-38557953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs535957602	chr7:38558024-38558025	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs552981481	chr7:38558058-38558059	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs191519043	chr7:38558060-38558061	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544916628	chr7:38558071-38558072	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558402442	chr7:38558095-38558096	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs543452878	chr7:38558123-38558124	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs544351928	chr7:38558128-38558129	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs560913522	chr7:38558141-38558142	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576298774	chr7:38558162-38558163	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs529434678	chr7:38558187-38558188	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542730683	chr7:38558190-38558191	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs6952029	chr7:38558192-38558193	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs565242567	chr7:38558221-38558222	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs377395928	chr7:38558264-38558265	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs117392407	chr7:38558267-38558268	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532448944	chr7:38558347-38558348	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs571926234	chr7:38558430-38558431	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs547847539	chr7:38558448-38558449	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs182445149	chr7:38558519-38558520	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs62443507	chr7:38558543-38558544	Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs536380225	chr7:38558555-38558556	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs371573309	chr7:38558567-38558568	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs538199947	chr7:38558576-38558577	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs146808423	chr7:38558586-38558587	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs575190344	chr7:38558594-38558595	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs564864377	chr7:38558607-38558608	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs537744701	chr7:38558611-38558612	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs140488656	chr7:38558647-38558648	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574533124	chr7:38558745-38558746	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs150439059	chr7:38558754-38558755	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs187812959	chr7:38558784-38558785	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs967022	chr7:38558805-38558806	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs138144214	chr7:38558820-38558821	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs565270534	chr7:38558891-38558892	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs531284817	chr7:38558927-38558928	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs73694533	chr7:38559005-38559006	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs567470129	chr7:38559059-38559060	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs68112925	chr7:38559069-38559070	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs375801698	chr7:38559070-38559071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs561545261	chr7:38559089-38559090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs149138439	chr7:38559129-38559130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs114260012	chr7:38559154-38559155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs566189836	chr7:38559231-38559232	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs538334878	chr7:38559257-38559258	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs551800516	chr7:38559312-38559313	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs568735903	chr7:38559314-38559315	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:38557800-38558800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr7:38558000-38558200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr7:38558000-38558600	Enhancers	Muscle Satellite Cultured Cells	--
4	chr7:38558400-38558800	Enhancers	NHDF-Ad	bronchial
5	chr7:38558800-38560000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:38560000-38560800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:38560800-38562600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr7:38562000-38562200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr7:38563800-38564200	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr7:38563800-38578400	Weak transcription	Aorta	Aorta
11	chr7:38564200-38580800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr7:38564800-38578400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:38569000-38569200	Enhancers	Pancreas	Pancrea
14	chr7:38569600-38574000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr7:38570000-38571000	Enhancers	Fetal Heart	heart
16	chr7:38570000-38571000	Enhancers	HUVEC	blood vessel
17	chr7:38570200-38570400	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr7:38570200-38570600	Enhancers	Spleen	Spleen
19	chr7:38570200-38570800	Enhancers	Right Atrium	heart
20	chr7:38570400-38571000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr7:38570400-38575400	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr7:38570600-38571000	Enhancers	H1 Cell Line	embryonic stem cell
23	chr7:38570600-38571000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:38570600-38571000	Genic enhancers	Spleen	Spleen
25	chr7:38570800-38572400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr7:38571000-38573400	Weak transcription	Fetal Heart	heart
27	chr7:38571000-38574800	Weak transcription	Spleen	Spleen
28	chr7:38572400-38573200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr7:38572600-38573800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr7:38573200-38574600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:38573400-38573600	Enhancers	Fetal Heart	heart
32	chr7:38573800-38574800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr7:38573800-38575600	Enhancers	Fetal Brain Male	brain
34	chr7:38574000-38575200	Enhancers	Cortex derived primary cultured neurospheres	brain
35	chr7:38574400-38575000	Enhancers	Brain Germinal Matrix	brain
36	chr7:38574400-38575200	Enhancers	Fetal Brain Female	brain
37	chr7:38574600-38575000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr7:38575000-38579200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr7:38575400-38575600	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr7:38578400-38578600	ZNF genes & repeats	Aorta	Aorta
41	chr7:38578400-38580200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr7:38578600-38579200	Weak transcription	Aorta	Aorta
43	chr7:38579200-38579400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr7:38579400-38580000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr7:38579400-38580200	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr7:38579400-38580200	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr7:38579400-38580200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr7:38579400-38580200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr7:38579400-38586800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr7:38579600-38580200	Enhancers	ES-I3 Cell Line	embryonic stem cell

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