Variant report

Variant	nsv1033155
Chromosome Location	chr7:70712368-70757929
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:90)
CpG islands
(count:123)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:90 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:70734244-70734559	HepG2	liver:	n/a	chr7:70734403-70734414 chr7:70734424-70734435
2	CEBPB	chr7:70724564-70724762	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr7:70716604-70717131	MCF-7	breast:	n/a	n/a
4	CEBPZ	chr7:70747253-70747255	HepG2	liver:	n/a	n/a
5	CHD2	chr7:70713141-70713347	K562	blood:	n/a	n/a
6	CTCF	chr7:70729020-70729170	GM12878	blood:	n/a	chr7:70729143-70729156
7	CTCF	chr7:70752357-70752421	GM13976	blood:	n/a	n/a
8	CTCF	chr7:70732820-70732970	MCF-7	breast:	n/a	chr7:70732908-70732916
9	CTCF	chr7:70732816-70732926	MCF-7	breast:	n/a	chr7:70732908-70732916
10	CTCF	chr7:70732791-70733152	MCF-7	breast:	n/a	chr7:70732908-70732916
11	CTCF	chr7:70732800-70732950	MCF-7	breast:	n/a	chr7:70732908-70732916
12	CTCF	chr7:70732899-70732942	MCF-7	breast:	n/a	chr7:70732908-70732916
13	CTCF	chr7:70732883-70732940	MCF-7	breast:	n/a	chr7:70732908-70732916
14	CTCF	chr7:70732872-70732924	K562	blood:	n/a	chr7:70732908-70732916
15	CTCF	chr7:70714334-70714353	K562	blood:	n/a	n/a
16	CTCF	chr7:70732780-70732930	WERI-Rb-1	eye:	n/a	chr7:70732908-70732916
17	CTCF	chr7:70732807-70732940	H1-hESC	embryonic stem cell:	n/a	chr7:70732908-70732916
18	CTCF	chr7:70732714-70733002	H1-hESC	embryonic stem cell:	n/a	chr7:70732908-70732916
19	E2F4	chr7:70717790-70717990	MCF10A-Er-Src	breast:	n/a	n/a
20	ELF1	chr7:70750608-70750837	K562	blood:	n/a	chr7:70750707-70750720
21	EP300	chr7:70716456-70717202	MCF-7	breast:	n/a	n/a
22	FOSL2	chr7:70716618-70717234	MCF-7	breast:	n/a	n/a
23	FOSL2	chr7:70716697-70717123	MCF-7	breast:	n/a	n/a
24	FOXA1	chr7:70716696-70717085	T-47D	breast:	n/a	n/a
25	FOXA1	chr7:70716715-70717057	T-47D	breast:	n/a	n/a
26	FOXM1	chr7:70716562-70717174	MCF-7	breast:	n/a	n/a
27	FOXM1	chr7:70716549-70717161	MCF-7	breast:	n/a	n/a
28	GABPA	chr7:70716556-70717175	MCF-7	breast:	n/a	n/a
29	GATA3	chr7:70716299-70717211	MCF-7	breast:	n/a	chr7:70717185-70717194
30	GATA3	chr7:70716670-70717031	MCF-7	breast:	n/a	n/a
31	GATA3	chr7:70716335-70717288	MCF-7	breast:	n/a	chr7:70717185-70717194
32	GATA3	chr7:70716582-70717076	MCF-7	breast:	n/a	n/a
33	GATA3	chr7:70716593-70717005	T-47D	breast:	n/a	n/a
34	HDAC2	chr7:70716439-70717195	MCF-7	breast:	n/a	n/a
35	HDAC2	chr7:70716635-70717063	MCF-7	breast:	n/a	n/a
36	IRF1	chr7:70715199-70715240	K562	blood:	n/a	n/a
37	IRF3	chr7:70738613-70738617	GM12878	blood:	n/a	n/a
38	JUND	chr7:70716627-70716966	T-47D	breast:	n/a	n/a
39	JUND	chr7:70716527-70717142	MCF-7	breast:	n/a	n/a
40	KAP1	chr7:70737446-70737764	HEK293	kidney:	n/a	n/a
41	MAFK	chr7:70738413-70738627	HepG2	liver:	n/a	chr7:70738524-70738540 chr7:70738528-70738539
42	MAFK	chr7:70757432-70757652	HepG2	liver:	n/a	n/a
43	MAFK	chr7:70756134-70756265	IMR90	lung:	n/a	n/a
44	MAFK	chr7:70757537-70757615	HepG2	liver:	n/a	n/a
45	MAX	chr7:70720688-70720935	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr7:70731934-70732212	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr7:70716492-70717176	MCF-7	breast:	n/a	n/a
48	MAZ	chr7:70732814-70732898	K562	blood:	n/a	n/a
49	MAZ	chr7:70730780-70730799	HepG2	liver:	n/a	n/a
50	MYC	chr7:70716793-70717013	MCF-7	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:70714201-70714251	NHDF-neo	bronchial:	n/a
2	chr7:70714201-70714251	NHDF-neo	bronchial:	n/a
3	chr7:70746877-70746927	HCT-116	colon:	n/a
4	chr7:70714201-70714251	T-47D	breast:	n/a
5	chr7:70746877-70746927	Hela-S3	cervix:	n/a
6	chr7:70746877-70746927	SK-N-SH	brain:	n/a
7	chr7:70746877-70746927	U87	brain:	n/a
8	chr7:70714201-70714251	PFSK-1	brain:	n/a
9	chr7:70746877-70746927	HRCEpiC	kidney:	n/a
10	chr7:70746877-70746927	BJ	skin:	n/a
11	chr7:70746877-70746927	AG09319	gingival:	n/a
12	chr7:70746877-70746927	SK-N-MC	brain:	n/a
13	chr7:70714201-70714251	BJ	skin:	n/a
14	chr7:70714201-70714251	SKMC	muscle:	n/a
15	chr7:70714201-70714251	HUVEC	blood vessel:	n/a
16	chr7:70746877-70746927	BE2_C	brain:	n/a
17	chr7:70714201-70714251	MCF-7	breast:	n/a
18	chr7:70714201-70714251	RPTEC	kidney:	n/a
19	chr7:70746877-70746927	HMEC	breast:	n/a
20	chr7:70714201-70714251	HIPEpiC	eye:	n/a
21	chr7:70746877-70746927	Caco-2	colon:	n/a
22	chr7:70714201-70714251	ProgFib	skin:	n/a
23	chr7:70714201-70714251	Jurkat	blood:	n/a
24	chr7:70746877-70746927	AG10803	skin:	n/a
25	chr7:70714201-70714251	U87	brain:	n/a
26	chr7:70714201-70714251	Caco-2	colon:	n/a
27	chr7:70746877-70746927	HEEpiC	esophagus:	n/a
28	chr7:70714201-70714251	HAEpiC	amniotic membrane:	n/a
29	chr7:70746877-70746927	HNPCEpiC	eye:	n/a
30	chr7:70746877-70746927	GM12878	blood:	n/a
31	chr7:70746877-70746927	PFSK-1	brain:	n/a
32	chr7:70714201-70714251	AG09309	skin:	n/a
33	chr7:70746877-70746927	MCF-7	breast:	n/a
34	chr7:70714201-70714251	NHBE	bronchial:	n/a
35	chr7:70746877-70746927	NHBE	bronchial:	n/a
36	chr7:70746877-70746927	HIPEpiC	eye:	n/a
37	chr7:70714201-70714251	HRPEpiC	eye:	n/a
38	chr7:70746877-70746927	HCPEpiC	choroid plexus:	n/a
39	chr7:70746877-70746927	IMR90	lung:	fetal
40	chr7:70746877-70746927	Jurkat	blood:	n/a
41	chr7:70714201-70714251	AG04449	skin:	fetal
42	chr7:70746877-70746927	GM12891	blood:	n/a
43	chr7:70714201-70714251	AG10803	skin:	n/a
44	chr7:70746877-70746927	SKMC	muscle:	n/a
45	chr7:70714201-70714251	HMEC	breast:	n/a
46	chr7:70714201-70714251	IMR90	lung:	fetal
47	chr7:70714201-70714251	HCM	heart:	n/a
48	chr7:70746877-70746927	MCF10A-Er-Src	breast:	n/a
49	chr7:70746877-70746927	GM19239	blood:	n/a
50	chr7:70714201-70714251	HNPCEpiC	eye:	n/a

No data

Variant related genes	Relation type
WBSCR17	TF binding region
WBSCR17	CpG island

Extended variants
information (count: 1993 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1993 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577671048	chr7:70712407-70712408	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs190313417	chr7:70712414-70712415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182625782	chr7:70712481-70712482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543936877	chr7:70712529-70712530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565243290	chr7:70712545-70712546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs532602776	chr7:70712563-70712564	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188835720	chr7:70712570-70712571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs192880994	chr7:70712597-70712598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530452226	chr7:70712730-70712731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs79207044	chr7:70712761-70712762	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs570279231	chr7:70712778-70712779	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537241859	chr7:70712808-70712809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559069686	chr7:70712812-70712813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571014947	chr7:70712815-70712816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs546771435	chr7:70712836-70712837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs2867047	chr7:70712880-70712881	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs377722793	chr7:70712909-70712910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs371346165	chr7:70712910-70712911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs183486477	chr7:70712927-70712928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145546670	chr7:70712931-70712932	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148181982	chr7:70712950-70712951	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576246777	chr7:70712966-70712967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs188776605	chr7:70712973-70712974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs376886424	chr7:70712990-70712991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192382341	chr7:70712997-70712998	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541524298	chr7:70713017-70713018	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs114627359	chr7:70713031-70713032	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs530114496	chr7:70713083-70713084	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183668067	chr7:70713084-70713085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs554478232	chr7:70713115-70713116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570265266	chr7:70713133-70713134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs531189648	chr7:70713145-70713146	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs552521077	chr7:70713165-70713166	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370303210	chr7:70713172-70713173	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs555943682	chr7:70713173-70713174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188087317	chr7:70713252-70713253	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs191794382	chr7:70713263-70713264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs553444315	chr7:70713274-70713275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565374571	chr7:70713303-70713304	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112543746	chr7:70713315-70713316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554503195	chr7:70713333-70713334	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184752332	chr7:70713371-70713372	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543667014	chr7:70713404-70713405	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558822633	chr7:70713453-70713454	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60583544	chr7:70713575-70713576	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs397969474	chr7:70713583-70713584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs190405274	chr7:70713590-70713591	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541585935	chr7:70713736-70713737	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568030914	chr7:70713748-70713749	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs559879251	chr7:70713784-70713785	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
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
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
Follicular lymphoma	20505157	CNVD
Biliary cancer	19435499	CNVD
Williams-beuren syndrome	22470819	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	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
T-cell prolymphocytic leukemia	17713554	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
Malignant fibrous histiocytomas	21085701	CNVD
Astrocytoma	22246337	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	16461572	CNVD
Acute monocytic leukemia	16498392	CNVD
Salivary gland tumor	18059337	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	21911935	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Neurodevelopmental disorder	22521361	CNVD
Renal cell carcinoma	18765545	CNVD
Chordoma	18071362	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:70701600-70720400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:70702200-70713600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:70702200-70719600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:70703600-70713800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr7:70703800-70713600	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr7:70704000-70713600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:70707200-70713600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:70709200-70713600	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr7:70709400-70718600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr7:70710400-70731800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr7:70710600-70712400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr7:70710600-70713800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:70712400-70717800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:70713600-70714000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr7:70713600-70714200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:70713600-70714200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr7:70713600-70714200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:70713600-70714600	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr7:70713600-70714800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr7:70713800-70715200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr7:70713800-70715600	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr7:70714000-70717400	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr7:70714200-70717800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr7:70714200-70719000	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr7:70714200-70720000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr7:70714600-70715600	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chr7:70714800-70718800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr7:70715200-70720200	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr7:70715600-70716000	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr7:70715600-70716000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr7:70715600-70718200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr7:70715600-70719600	Weak transcription	Fetal Muscle Leg	muscle
33	chr7:70715800-70717000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr7:70716800-70717200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr7:70717400-70718200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
36	chr7:70717800-70718600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr7:70717800-70722000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr7:70718200-70719400	Strong transcription	iPS-20b Cell Line	embryonic stem cell
39	chr7:70718600-70719000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:70718600-70719200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr7:70718600-70721800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr7:70718800-70721000	Enhancers	Fetal Brain Male	brain
43	chr7:70718800-70721600	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr7:70719000-70721000	Enhancers	H1 Cell Line	embryonic stem cell
45	chr7:70719200-70719800	Enhancers	Placenta Amnion	Placenta Amnion
46	chr7:70719400-70719600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
47	chr7:70719600-70719800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr7:70719600-70720200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr7:70719600-70720600	Enhancers	Fetal Heart	heart
50	chr7:70719600-70720800	Enhancers	Fetal Muscle Leg	muscle

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