Variant report

Variant	nsv5
Chromosome Location	chr7:96451352-96494110
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:96462504-96463681	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:96452686-96452882	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:96461364-96461771	HepG2	liver:	n/a	n/a
4	ATF2	chr7:96466802-96467307	GM12878	blood:	n/a	n/a
5	ATF2	chr7:96466878-96467356	GM12878	blood:	n/a	n/a
6	ATF3	chr7:96455403-96455730	HCT-116	colon:	n/a	n/a
7	ATF3	chr7:96455501-96455675	HepG2	liver:	n/a	n/a
8	BACH1	chr7:96452279-96452346	K562	blood:	n/a	n/a
9	BACH1	chr7:96486956-96487015	K562	blood:	n/a	n/a
10	BATF	chr7:96452678-96452863	GM12878	blood:	n/a	chr7:96452790-96452801
11	BATF	chr7:96466820-96467279	GM12878	blood:	n/a	n/a
12	BATF	chr7:96452660-96452871	GM12878	blood:	n/a	chr7:96452790-96452801
13	BATF	chr7:96466848-96467246	GM12878	blood:	n/a	n/a
14	BCL11A	chr7:96466966-96467247	GM12878	blood:	n/a	n/a
15	BHLHE40	chr7:96462915-96463473	HepG2	liver:	n/a	n/a
16	CBX3	chr7:96455493-96455742	HCT-116	colon:	n/a	n/a
17	CEBPB	chr7:96467881-96468155	HepG2	liver:	n/a	n/a
18	CEBPB	chr7:96485085-96485322	HepG2	liver:	n/a	chr7:96485207-96485218
19	CEBPB	chr7:96462896-96463607	HepG2	liver:	n/a	chr7:96463101-96463113
20	CEBPB	chr7:96489541-96489582	A549	lung:	n/a	n/a
21	CEBPB	chr7:96455298-96455753	HCT-116	colon:	n/a	chr7:96455573-96455584
22	CEBPB	chr7:96492420-96492569	HepG2	liver:	n/a	n/a
23	CEBPB	chr7:96456717-96456917	HepG2	liver:	n/a	n/a
24	CEBPB	chr7:96455302-96455743	HCT-116	colon:	n/a	chr7:96455573-96455584
25	CEBPB	chr7:96461695-96461862	HepG2	liver:	n/a	n/a
26	CEBPB	chr7:96455452-96455669	K562	blood:	n/a	chr7:96455573-96455584
27	CEBPB	chr7:96455430-96455695	K562	blood:	n/a	chr7:96455573-96455584
28	CEBPB	chr7:96455407-96455732	HepG2	liver:	n/a	chr7:96455573-96455584
29	CEBPB	chr7:96455422-96455777	Hela-S3	cervix:	n/a	chr7:96455573-96455584
30	CEBPB	chr7:96455494-96455634	HepG2	liver:	n/a	chr7:96455573-96455584
31	CTCF	chr7:96467935-96468041	MCF-7	breast:	n/a	chr7:96467985-96467998 chr7:96467990-96467998
32	CTCF	chr7:96489473-96489541	GM13977	blood:	n/a	n/a
33	CTCF	chr7:96467940-96468090	Caco-2	colon:	n/a	chr7:96467985-96467998 chr7:96467990-96467998
34	CTCF	chr7:96467980-96468130	MCF-7	breast:	n/a	chr7:96467985-96467998 chr7:96467990-96467998
35	CTCF	chr7:96457060-96457210	K562	blood:	n/a	n/a
36	CTCF	chr7:96457020-96457170	SK-N-SH_RA	brain:	n/a	n/a
37	CTCF	chr7:96457120-96457270	BE2_C	brain:	n/a	chr7:96457232-96457245 chr7:96457192-96457213 chr7:96457197-96457215
38	CTCF	chr7:96457120-96457270	Caco-2	colon:	n/a	chr7:96457232-96457245 chr7:96457192-96457213 chr7:96457197-96457215
39	CTCF	chr7:96457160-96457310	MCF-7	breast:	n/a	chr7:96457232-96457245 chr7:96457192-96457213 chr7:96457197-96457215
40	CTCF	chr7:96457153-96457222	MCF-7	breast:	n/a	chr7:96457192-96457213 chr7:96457197-96457215
41	CTCF	chr7:96467936-96468043	MCF-7	breast:	n/a	chr7:96467985-96467998 chr7:96467990-96467998
42	CTCF	chr7:96454800-96454950	GM12873	blood:	n/a	n/a
43	CTCF	chr7:96467960-96468110	HepG2	liver:	n/a	chr7:96467985-96467998 chr7:96467990-96467998
44	CTCF	chr7:96467964-96468031	MCF-7	breast:	n/a	chr7:96467985-96467998 chr7:96467990-96467998
45	CTCF	chr7:96467971-96468035	MCF-7	breast:	n/a	chr7:96467985-96467998 chr7:96467990-96467998
46	CTCF	chr7:96461780-96461930	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr7:96457067-96457353	K562	blood:	n/a	chr7:96457232-96457245 chr7:96457192-96457213 chr7:96457197-96457215
48	CTCF	chr7:96457069-96457313	K562	blood:	n/a	chr7:96457232-96457245 chr7:96457192-96457213 chr7:96457197-96457215
49	CTCF	chr7:96457160-96457310	HepG2	liver:	n/a	chr7:96457232-96457245 chr7:96457192-96457213 chr7:96457197-96457215
50	CTCF	chr7:96457068-96457348	K562	blood:	n/a	chr7:96457232-96457245 chr7:96457192-96457213 chr7:96457197-96457215

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:96483662-96483712	SK-N-MC	brain:	n/a
2	chr7:96483662-96483712	K562	blood:	n/a
3	chr7:96483662-96483712	A549	lung:	n/a
4	chr7:96483662-96483712	NHBE	bronchial:	n/a
5	chr7:96483662-96483712	AG09309	skin:	n/a
6	chr7:96483662-96483712	HepG2	liver:	n/a
7	chr7:96483662-96483712	AG10803	skin:	n/a
8	chr7:96483662-96483712	MCF10A-Er-Src	breast:	n/a
9	chr7:96483662-96483712	SK-N-SH_RA	brain:	n/a
10	chr7:96483662-96483712	GM12878	blood:	n/a
11	chr7:96483662-96483712	AG09319	gingival:	n/a
12	chr7:96483662-96483712	NT2-D1	testis:	n/a
13	chr7:96483662-96483712	PFSK-1	brain:	n/a
14	chr7:96483662-96483712	HCF	heart:	n/a
15	chr7:96483662-96483712	AG04450	lung:	fetal
16	chr7:96483662-96483712	Hela-S3	cervix:	n/a
17	chr7:96483662-96483712	ovcar-3	ovarian:	n/a
18	chr7:96483662-96483712	GM12891	blood:	n/a
19	chr7:96483662-96483712	GM12892	blood:	n/a
20	chr7:96483662-96483712	HEK293	kidney:	embryo
21	chr7:96483662-96483712	U87	brain:	n/a
22	chr7:96483662-96483712	LNCaP	prostate:	n/a
23	chr7:96483662-96483712	HAEpiC	amniotic membrane:	n/a
24	chr7:96483662-96483712	PANC-1	pancreas:	n/a
25	chr7:96483662-96483712	NH-A	brain:	n/a
26	chr7:96483662-96483712	SAEC	small airway:	n/a
27	chr7:96483662-96483712	NB4	blood:	n/a
28	chr7:96483662-96483712	Hepatocyte	liver:	n/a
29	chr7:96483662-96483712	HIPEpiC	eye:	n/a
30	chr7:96483662-96483712	HMEC	breast:	n/a
31	chr7:96483662-96483712	HEEpiC	esophagus:	n/a
32	chr7:96483662-96483712	Jurkat	blood:	n/a
33	chr7:96483662-96483712	ProgFib	skin:	n/a
34	chr7:96483662-96483712	GM19239	blood:	n/a
35	chr7:96483662-96483712	BE2_C	brain:	n/a
36	chr7:96483662-96483712	HRPEpiC	eye:	n/a
37	chr7:96483662-96483712	IMR90	lung:	fetal
38	chr7:96483662-96483712	SK-N-SH	brain:	n/a
39	chr7:96483662-96483712	MCF-7	breast:	n/a
40	chr7:96483662-96483712	HCM	heart:	n/a
41	chr7:96483662-96483712	BJ	skin:	n/a
42	chr7:96483662-96483712	HCPEpiC	choroid plexus:	n/a
43	chr7:96483662-96483712	HRE	kidney:	n/a
44	chr7:96483662-96483712	HRCEpiC	kidney:	n/a
45	chr7:96483662-96483712	HPAEpiC	pulmonary alveolar:	n/a
46	chr7:96483662-96483712	CMK	blood:	n/a
47	chr7:96483662-96483712	AG04449	skin:	fetal
48	chr7:96483662-96483712	ECC-1	luminal epithelium:	n/a
49	chr7:96483662-96483712	NHDF-neo	bronchial:	n/a
50	chr7:96483662-96483712	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:96454800..96457390-chr7:96459859..96461743,2	K562	blood:
2	chr7:96473083..96476010-chr7:96482682..96485380,3	K562	blood:
3	chr7:96473083..96476010-chr7:96482682..96485380,3	K562	blood:
4	chr7:96409535..96411898-chr7:96450818..96453069,2	K562	blood:
5	chr7:96287815..96289788-chr7:96460345..96461965,2	K562	blood:
6	chr7:96454800..96457390-chr7:96459859..96461743,2	K562	blood:

Variant related genes	Relation type
MARK2P10	TF binding region
MARK2P10	CpG island

Extended variants
information (count: 744 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:744 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74548843	chr7:96451398-96451399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs201185921	chr7:96451413-96451414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141928472	chr7:96451421-96451422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561068454	chr7:96451470-96451471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs574557984	chr7:96451482-96451483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116610225	chr7:96451515-96451516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1212147	chr7:96451542-96451543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs541927258	chr7:96451547-96451548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190878562	chr7:96451592-96451593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs532348225	chr7:96451609-96451610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs552435865	chr7:96451724-96451725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562375438	chr7:96451735-96451736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531312976	chr7:96451745-96451746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1403186	chr7:96451758-96451759	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs150529576	chr7:96451772-96451773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs552423336	chr7:96451798-96451799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2922964	chr7:96451800-96451801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs139914079	chr7:96451806-96451807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538395013	chr7:96451807-96451808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115738016	chr7:96451819-96451820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs386715943	chr7:96451870-96451871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113636484	chr7:96451871-96451872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs10251989	chr7:96451924-96451925	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs189038835	chr7:96451972-96451973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78445539	chr7:96451973-96451974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs375658023	chr7:96451986-96451987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192314245	chr7:96452007-96452008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs535611096	chr7:96452030-96452031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs377736570	chr7:96452038-96452039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs574594757	chr7:96452039-96452040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369001282	chr7:96452073-96452074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs377071063	chr7:96452080-96452081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369713247	chr7:96452087-96452088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184470830	chr7:96452118-96452119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs553214037	chr7:96452145-96452146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563276650	chr7:96452158-96452159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530608623	chr7:96452161-96452162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77520112	chr7:96452207-96452208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142288007	chr7:96452229-96452230	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs66819162	chr7:96452231-96452232	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs75496662	chr7:96452232-96452233	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs10533103	chr7:96452242-96452243	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187280100	chr7:96452245-96452246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200775818	chr7:96452253-96452254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs58502395	chr7:96452254-96452255	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561666493	chr7:96452268-96452269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs75061993	chr7:96452270-96452271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547500377	chr7:96452290-96452291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs145849278	chr7:96452302-96452303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75731719	chr7:96452321-96452322	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Glioblastoma multiforme	21750150	CNVD
Cancer	21183584	CNVD
Hepatocellular carcinoma	16750200	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
Metanephric adenoma	20802469	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Schizophrenia	17879154	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	20858243	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
lymphocytic leukemia	21291569	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myoclonus-dystonia	17898012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164920	CNVD
abnormal development	18461090	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:144 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:96450000-96453000	Weak transcription	HMEC	breast
2	chr7:96450000-96454000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr7:96450200-96452200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr7:96452200-96452600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr7:96452200-96453200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:96452200-96453400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr7:96452400-96453200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:96452400-96453400	Enhancers	NHEK	skin
9	chr7:96452600-96454600	Enhancers	Fetal Brain Female	brain
10	chr7:96453000-96453400	Enhancers	HMEC	breast
11	chr7:96453200-96453800	Enhancers	Fetal Brain Male	brain
12	chr7:96454000-96454800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr7:96454600-96455800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
14	chr7:96455600-96455800	Enhancers	HepG2	liver
15	chr7:96456000-96456600	Weak transcription	HepG2	liver
16	chr7:96456600-96456800	Enhancers	HepG2	liver
17	chr7:96456800-96457600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:96456800-96461400	Weak transcription	HepG2	liver
19	chr7:96456800-96463200	Weak transcription	Stomach Mucosa	stomach
20	chr7:96461000-96461200	Enhancers	Osteobl	bone
21	chr7:96461000-96461800	Enhancers	Fetal Stomach	stomach
22	chr7:96461200-96461800	Enhancers	Brain Germinal Matrix	brain
23	chr7:96461200-96461800	Weak transcription	Osteobl	bone
24	chr7:96461200-96462000	Enhancers	Ovary	ovary
25	chr7:96461400-96462200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr7:96461400-96464000	Enhancers	HepG2	liver
27	chr7:96461600-96462000	Enhancers	NHDF-Ad	bronchial
28	chr7:96461600-96463800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
29	chr7:96461800-96462000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:96461800-96462000	Enhancers	Spleen	Spleen
31	chr7:96461800-96462600	Weak transcription	Fetal Stomach	stomach
32	chr7:96461800-96462600	Enhancers	Osteobl	bone
33	chr7:96461800-96463000	Weak transcription	Brain Germinal Matrix	brain
34	chr7:96462000-96462800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:96462000-96463000	Weak transcription	Ovary	ovary
36	chr7:96462000-96463200	Weak transcription	NHDF-Ad	bronchial
37	chr7:96462000-96466200	Weak transcription	Spleen	Spleen
38	chr7:96462200-96463000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr7:96462600-96463000	Weak transcription	Osteobl	bone
40	chr7:96462600-96463600	Enhancers	Fetal Kidney	kidney
41	chr7:96462800-96463800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr7:96463000-96463200	Enhancers	Brain Germinal Matrix	brain
43	chr7:96463000-96463400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr7:96463000-96463400	Enhancers	Ovary	ovary
45	chr7:96463000-96463600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr7:96463000-96463600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr7:96463000-96463600	Enhancers	Colon Smooth Muscle	Colon
48	chr7:96463000-96463600	Enhancers	A549	lung
49	chr7:96463000-96463800	Enhancers	Osteobl	bone
50	chr7:96463200-96463400	Enhancers	Fetal Stomach	stomach

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