Variant report

Variant	nsv1017114
Chromosome Location	chr7:107692403-107720162
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:326)
CpG islands
(count:244)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:326 , 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	chr7:107719118-107719323	K562	blood:	n/a	n/a
2	ARID3A	chr7:107718374-107718556	K562	blood:	n/a	n/a
3	ARID3A	chr7:107704284-107704369	HepG2	liver:	n/a	n/a
4	BATF	chr7:107703832-107704196	GM12878	blood:	n/a	n/a
5	BATF	chr7:107703840-107704183	GM12878	blood:	n/a	n/a
6	BCL11A	chr7:107703874-107704176	GM12878	blood:	n/a	n/a
7	BHLHE40	chr7:107693838-107694004	K562	blood:	n/a	n/a
8	BHLHE40	chr7:107703883-107704262	GM12878	blood:	n/a	n/a
9	BHLHE40	chr7:107696149-107696450	HepG2	liver:	n/a	n/a
10	BHLHE40	chr7:107718630-107718852	K562	blood:	n/a	n/a
11	BHLHE40	chr7:107696792-107696906	A549	lung:	n/a	n/a
12	BHLHE40	chr7:107703335-107703366	K562	blood:	n/a	n/a
13	BHLHE40	chr7:107702786-107703341	GM12878	blood:	n/a	n/a
14	CBX3	chr7:107719994-107721103	K562	blood:	n/a	n/a
15	CEBPB	chr7:107693620-107693740	K562	blood:	n/a	chr7:107693667-107693678
16	CEBPB	chr7:107718544-107718715	K562	blood:	n/a	n/a
17	CEBPB	chr7:107704092-107704450	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:107693608-107693791	HepG2	liver:	n/a	chr7:107693667-107693678
19	CEBPB	chr7:107696091-107696203	HepG2	liver:	n/a	n/a
20	CEBPB	chr7:107707036-107707238	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr7:107710193-107710332	K562	blood:	n/a	n/a
22	CEBPB	chr7:107692740-107693044	HepG2	liver:	n/a	chr7:107692897-107692908
23	CEBPB	chr7:107692748-107693029	IMR90	lung:	n/a	chr7:107692897-107692908
24	CEBPB	chr7:107692749-107693055	K562	blood:	n/a	chr7:107692897-107692908
25	CEBPB	chr7:107692793-107693007	A549	lung:	n/a	chr7:107692897-107692908
26	CHD2	chr7:107703891-107704239	GM12878	blood:	n/a	n/a
27	CHD2	chr7:107704959-107705123	GM12878	blood:	n/a	n/a
28	CHD2	chr7:107714368-107714445	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr7:107704061-107704122	GM10248	blood:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
30	CTCF	chr7:107703960-107704110	HMEC	breast:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
31	CTCF	chr7:107703380-107703530	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr7:107704047-107704154	GM12892	blood:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
33	CTCF	chr7:107704060-107704210	GM12878	blood:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
34	CTCF	chr7:107704060-107704210	GM12865	blood:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
35	CTCF	chr7:107703280-107703430	HEK293	kidney:	n/a	n/a
36	CTCF	chr7:107710713-107710891	K562	blood:	n/a	chr7:107710716-107710724
37	CTCF	chr7:107703360-107703510	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr7:107703960-107704110	HEEpiC	esophagus:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
39	CTCF	chr7:107718600-107718750	K562	blood:	n/a	n/a
40	CTCF	chr7:107704020-107704170	GM12873	blood:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
41	CTCF	chr7:107703260-107703410	BE2_C	brain:	n/a	n/a
42	CTCF	chr7:107703280-107703430	K562	blood:	n/a	n/a
43	CTCF	chr7:107710773-107710872	K562	blood:	n/a	n/a
44	CTCF	chr7:107703940-107704090	SAEC	small airway:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
45	CTCF	chr7:107718654-107718781	K562	blood:	n/a	n/a
46	CTCF	chr7:107703907-107704250	GM12878	blood:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
47	CTCF	chr7:107718820-107718970	K562	blood:	n/a	n/a
48	CTCF	chr7:107703960-107704110	NHEK	skin:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
49	CTCF	chr7:107704040-107704190	GM06990	blood:	n/a	chr7:107704068-107704089 chr7:107704080-107704087
50	CTCF	chr7:107704040-107704190	HEEpiC	esophagus:	n/a	chr7:107704068-107704089 chr7:107704080-107704087

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:107704289-107704339	SAEC	small airway:	n/a
2	chr7:107719635-107719685	GM12878	blood:	n/a
3	chr7:107719635-107719685	U87	brain:	n/a
4	chr7:107700124-107700174	HPAEpiC	pulmonary alveolar:	n/a
5	chr7:107700124-107700174	H1-hESC	embryonic stem cell:	embryo
6	chr7:107704289-107704339	T-47D	breast:	n/a
7	chr7:107704289-107704339	GM12892	blood:	n/a
8	chr7:107719635-107719685	AoSMC	blood vessel:	n/a
9	chr7:107700124-107700174	HCPEpiC	choroid plexus:	n/a
10	chr7:107700124-107700174	Caco-2	colon:	n/a
11	chr7:107719635-107719685	SK-N-MC	brain:	n/a
12	chr7:107704289-107704339	Hela-S3	cervix:	n/a
13	chr7:107704289-107704339	HRE	kidney:	n/a
14	chr7:107708470-107708520	HAEpiC	amniotic membrane:	n/a
15	chr7:107719635-107719685	AG10803	skin:	n/a
16	chr7:107708470-107708520	HCM	heart:	n/a
17	chr7:107704289-107704339	HUVEC	blood vessel:	n/a
18	chr7:107700124-107700174	LNCaP	prostate:	n/a
19	chr7:107700124-107700174	HCT-116	colon:	n/a
20	chr7:107719635-107719685	SK-N-SH_RA	brain:	n/a
21	chr7:107700124-107700174	HMEC	breast:	n/a
22	chr7:107700124-107700174	Jurkat	blood:	n/a
23	chr7:107719635-107719685	H1-hESC	embryonic stem cell:	embryo
24	chr7:107700124-107700174	T-47D	breast:	n/a
25	chr7:107708470-107708520	ECC-1	luminal epithelium:	n/a
26	chr7:107719635-107719685	BE2_C	brain:	n/a
27	chr7:107704289-107704339	HAEpiC	amniotic membrane:	n/a
28	chr7:107700124-107700174	MCF10A-Er-Src	breast:	n/a
29	chr7:107704289-107704339	NHDF-neo	bronchial:	n/a
30	chr7:107704289-107704339	AoSMC	blood vessel:	n/a
31	chr7:107708470-107708520	AG04449	skin:	fetal
32	chr7:107704289-107704339	HEEpiC	esophagus:	n/a
33	chr7:107704289-107704339	SK-N-SH_RA	brain:	n/a
34	chr7:107704289-107704339	HCF	heart:	n/a
35	chr7:107700124-107700174	PFSK-1	brain:	n/a
36	chr7:107719635-107719685	PrEC	prostate:	n/a
37	chr7:107700124-107700174	AG10803	skin:	n/a
38	chr7:107700124-107700174	NH-A	brain:	n/a
39	chr7:107708470-107708520	AG09319	gingival:	n/a
40	chr7:107719635-107719685	GM19239	blood:	n/a
41	chr7:107700124-107700174	NB4	blood:	n/a
42	chr7:107708470-107708520	ProgFib	skin:	n/a
43	chr7:107719635-107719685	LNCaP	prostate:	n/a
44	chr7:107704289-107704339	AG10803	skin:	n/a
45	chr7:107700124-107700174	HEEpiC	esophagus:	n/a
46	chr7:107700124-107700174	Hela-S3	cervix:	n/a
47	chr7:107708470-107708520	HNPCEpiC	eye:	n/a
48	chr7:107708470-107708520	PFSK-1	brain:	n/a
49	chr7:107708470-107708520	IMR90	lung:	fetal
50	chr7:107704289-107704339	HNPCEpiC	eye:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:107689459..107691309-chr7:107692486..107694107,2	MCF-7	breast:
2	chr7:107719784..107721782-chr7:107727829..107731774,3	K562	blood:
3	chr7:107677483..107679632-chr7:107703067..107705427,2	K562	blood:
4	chr7:107703724..107706377-chr7:107714515..107716129,2	MCF-7	breast:
5	chr7:107716979..107718489-chr7:107727932..107729700,2	K562	blood:
6	chr7:107706468..107709689-chr7:107710215..107712909,3	K562	blood:
7	chr7:107693993..107696951-chr7:107697117..107699478,2	K562	blood:
8	chr7:107686762..107692628-chr7:107693774..107699382,6	K562	blood:
9	chr7:107706468..107709689-chr7:107710215..107712909,3	K562	blood:
10	chr7:107707012..107709867-chr7:107716740..107718585,2	K562	blood:
11	chr7:107693993..107696951-chr7:107697117..107699478,2	K562	blood:
12	chr7:107701556..107705912-chr7:107707647..107710680,4	K562	blood:
13	chr7:107129283..107132125-chr7:107690846..107692465,2	K562	blood:
14	chr7:107686762..107692628-chr7:107693774..107699382,6	K562	blood:
15	chr7:107714760..107717212-chr7:107718559..107721674,3	K562	blood:
16	chr7:107705705..107708395-chr7:107795206..107798922,3	K562	blood:
17	chr7:107705898..107709867-chr7:107715433..107718240,3	K562	blood:
18	chr7:107712773..107718092-chr7:107719257..107721672,4	K562	blood:
19	chr7:107719530..107722382-chr7:107729681..107732039,2	MCF-7	breast:
20	chr7:107714760..107717212-chr7:107718559..107721674,3	K562	blood:
21	chr7:107699191..107701387-chr7:107720831..107722439,2	K562	blood:
22	chr7:107712773..107718092-chr7:107719257..107721672,4	K562	blood:
23	chr7:107707012..107709867-chr7:107716740..107718585,2	K562	blood:

No data

Variant related genes	Relation type
LAMB4	TF binding region
LAMB4	CpG island
ENSG00000091128	chromatin interactions
ENSG00000091129	chromatin interactions

Extended variants
information (count: 1065 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1065 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533302499	chr7:107692406-107692407	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs61237166	chr7:107692411-107692412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565768652	chr7:107692415-107692416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528538666	chr7:107692436-107692437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs548281576	chr7:107692452-107692453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373673583	chr7:107692466-107692467	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs537241881	chr7:107692472-107692473	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375462065	chr7:107692488-107692489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182947815	chr7:107692501-107692502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147285482	chr7:107692545-107692546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs372436428	chr7:107692575-107692576	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs200812415	chr7:107692580-107692581	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs201305121	chr7:107692589-107692590	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377473114	chr7:107692637-107692638	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs202031134	chr7:107692638-107692639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376670405	chr7:107692648-107692649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528984661	chr7:107692661-107692662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149493645	chr7:107692681-107692682	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs369690971	chr7:107692702-107692703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs535495264	chr7:107692709-107692710	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs372337424	chr7:107692721-107692722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78814472	chr7:107692782-107692783	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575337564	chr7:107692817-107692818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs370227516	chr7:107692836-107692837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532614920	chr7:107692841-107692842	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs373718906	chr7:107692849-107692850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564332299	chr7:107692850-107692851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185874548	chr7:107692873-107692874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs112857089	chr7:107692921-107692922	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369498660	chr7:107692983-107692984	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540160208	chr7:107693009-107693010	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191178186	chr7:107693031-107693032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs528478294	chr7:107693044-107693045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572137766	chr7:107693055-107693056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs548221171	chr7:107693077-107693078	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs202133158	chr7:107693151-107693152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562038762	chr7:107693154-107693155	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs531062445	chr7:107693275-107693276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs183341777	chr7:107693320-107693321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76633647	chr7:107693437-107693438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs11487091	chr7:107693455-107693456	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs74610155	chr7:107693463-107693464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566434332	chr7:107693478-107693479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535433907	chr7:107693548-107693549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555385367	chr7:107693593-107693594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575225835	chr7:107693594-107693595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs375183013	chr7:107693648-107693649	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs537978487	chr7:107693657-107693658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs116123337	chr7:107693679-107693680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs577421108	chr7:107693689-107693690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	17053054	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Squamous cell cancer	20885788	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16397240	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Autism	19401682	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:275 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107686600-107703000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:107688200-107693000	Enhancers	Primary T cells from cord blood	blood
3	chr7:107690800-107692600	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr7:107691400-107692600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:107692200-107692600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr7:107692400-107692600	Enhancers	Fetal Stomach	stomach
7	chr7:107692600-107693200	Enhancers	HepG2	liver
8	chr7:107692800-107693000	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr7:107693200-107693600	Weak transcription	HepG2	liver
10	chr7:107693600-107696000	Enhancers	HepG2	liver
11	chr7:107694000-107694200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr7:107694200-107696200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:107695000-107695600	Enhancers	Stomach Mucosa	stomach
14	chr7:107695000-107695600	Enhancers	A549	lung
15	chr7:107695600-107696600	Enhancers	Placenta	Placenta
16	chr7:107695600-107697000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr7:107695800-107696800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr7:107696000-107696400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:107696000-107696400	Flanking Active TSS	HepG2	liver
20	chr7:107696000-107696800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr7:107696000-107697000	Enhancers	Fetal Heart	heart
22	chr7:107696200-107696400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr7:107696200-107696400	Enhancers	HSMMtube	muscle
24	chr7:107696200-107696600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr7:107696200-107696600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr7:107696200-107696600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr7:107696200-107696600	Enhancers	Fetal Muscle Leg	muscle
28	chr7:107696200-107696600	Enhancers	NHLF	lung
29	chr7:107696400-107696800	Enhancers	HepG2	liver
30	chr7:107696400-107697600	Enhancers	Fetal Muscle Trunk	muscle
31	chr7:107696400-107699200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr7:107696600-107697000	Weak transcription	Fetal Muscle Leg	muscle
33	chr7:107696600-107703000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr7:107696600-107703000	Weak transcription	NHLF	lung
35	chr7:107697000-107701400	Enhancers	Fetal Muscle Leg	muscle
36	chr7:107697600-107699000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr7:107697600-107701600	Enhancers	Fetal Stomach	stomach
38	chr7:107697800-107699200	Enhancers	Fetal Kidney	kidney
39	chr7:107698200-107698800	Enhancers	Fetal Lung	lung
40	chr7:107698400-107698600	Enhancers	Ovary	ovary
41	chr7:107698400-107698600	Enhancers	HSMMtube	muscle
42	chr7:107698600-107699800	Weak transcription	HSMMtube	muscle
43	chr7:107698600-107720000	Weak transcription	Right Atrium	heart
44	chr7:107698800-107699800	Weak transcription	Ovary	ovary
45	chr7:107698800-107700200	Weak transcription	Fetal Lung	lung
46	chr7:107699000-107700200	Enhancers	Fetal Muscle Trunk	muscle
47	chr7:107699200-107700200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr7:107699400-107701200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr7:107699800-107700600	Enhancers	Ovary	ovary
50	chr7:107699800-107701000	Enhancers	Adipose Nuclei	Adipose

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