Variant report

Variant	nsv817238
Chromosome Location	chr7:122325864-122371594
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:215)
CpG islands
(count:490)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:215 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:122335758-122336328	HepG2	liver:	n/a	n/a
2	ATF1	chr7:122328801-122328997	K562	blood:	n/a	n/a
3	BACH1	chr7:122328816-122328949	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr7:122365495-122365692	GM12878	blood:	n/a	n/a
5	BHLHE40	chr7:122350118-122350420	GM12878	blood:	n/a	n/a
6	BHLHE40	chr7:122361311-122361406	HepG2	liver:	n/a	n/a
7	CEBPB	chr7:122329697-122329956	HepG2	liver:	n/a	n/a
8	CEBPB	chr7:122334309-122334612	HepG2	liver:	n/a	chr7:122334450-122334463
9	CHD2	chr7:122335932-122336337	HepG2	liver:	n/a	n/a
10	CHD2	chr7:122329764-122329946	HepG2	liver:	n/a	n/a
11	CTCF	chr7:122331751-122331863	MCF-7	breast:	n/a	n/a
12	CTCF	chr7:122336056-122336239	HepG2	liver:	n/a	chr7:122336160-122336178 chr7:122336155-122336176 chr7:122336165-122336173
13	CTCF	chr7:122329440-122329590	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr7:122329520-122329670	HepG2	liver:	n/a	n/a
15	CTCF	chr7:122329920-122330070	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr7:122329500-122329650	RPTEC	kidney:	n/a	n/a
17	CTCF	chr7:122340260-122340410	AG09319	gingival:	n/a	n/a
18	CTCF	chr7:122329540-122329690	GM12864	blood:	n/a	n/a
19	CTCF	chr7:122329933-122330010	GM19240	blood:	n/a	n/a
20	CTCF	chr7:122329440-122329590	GM12865	blood:	n/a	n/a
21	CTCF	chr7:122329886-122330039	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr7:122331722-122331856	MCF-7	breast:	n/a	n/a
23	CTCF	chr7:122329780-122329930	GM12864	blood:	n/a	n/a
24	CTCF	chr7:122329520-122329670	MCF-7	breast:	n/a	n/a
25	CTCF	chr7:122329958-122329996	GM12891	blood:	n/a	n/a
26	CTCF	chr7:122329860-122330010	GM12872	blood:	n/a	n/a
27	CTCF	chr7:122329457-122329669	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr7:122336043-122336319	GM12878	blood:	n/a	chr7:122336160-122336178 chr7:122336155-122336176 chr7:122336165-122336173
29	CTCF	chr7:122329510-122329710	MCF-7	breast:	n/a	n/a
30	CTCF	chr7:122329500-122329650	HEK293	kidney:	n/a	n/a
31	CTCF	chr7:122329540-122329690	GM12874	blood:	n/a	n/a
32	CTCF	chr7:122329399-122330136	GM12878	blood:	n/a	n/a
33	CTCF	chr7:122329546-122329594	GM19238	blood:	n/a	n/a
34	CTCF	chr7:122329480-122329630	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr7:122329500-122329650	GM06990	blood:	n/a	n/a
36	CTCF	chr7:122329840-122329990	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr7:122329521-122329595	GM12878	blood:	n/a	n/a
38	CTCF	chr7:122329440-122329590	GM12872	blood:	n/a	n/a
39	CTCF	chr7:122329513-122329642	HepG2	liver:	n/a	n/a
40	CTCF	chr7:122336080-122336230	HepG2	liver:	n/a	chr7:122336160-122336178 chr7:122336155-122336176 chr7:122336165-122336173
41	CTCF	chr7:122329540-122329586	Medullo	brain:	n/a	n/a
42	CTCF	chr7:122329920-122330002	MCF-7	breast:	n/a	n/a
43	CTCF	chr7:122331724-122331865	MCF-7	breast:	n/a	n/a
44	CTCF	chr7:122336123-122336227	HepG2	liver:	n/a	chr7:122336160-122336178 chr7:122336155-122336176 chr7:122336165-122336173
45	CTCF	chr7:122329487-122329687	MCF-7	breast:	n/a	n/a
46	CTCF	chr7:122329555-122329675	MCF-7	breast:	n/a	n/a
47	CTCF	chr7:122329480-122329630	HCT-116	colon:	n/a	n/a
48	CTCF	chr7:122331731-122331738	HepG2	liver:	n/a	n/a
49	CTCF	chr7:122329540-122329690	HepG2	liver:	n/a	n/a
50	CTCF	chr7:122329660-122329810	RPTEC	kidney:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:122343409-122343459	GM12891	blood:	n/a
2	chr7:122338985-122339035	HNPCEpiC	eye:	n/a
3	chr7:122343409-122343459	GM12891	blood:	n/a
4	chr7:122338985-122339035	HNPCEpiC	eye:	n/a
5	chr7:122340281-122340331	ovcar-3	ovarian:	n/a
6	chr7:122338579-122338629	AG04449	skin:	fetal
7	chr7:122326807-122326857	AoSMC	blood vessel:	n/a
8	chr7:122326807-122326857	NHBE	bronchial:	n/a
9	chr7:122340193-122340243	AG10803	skin:	n/a
10	chr7:122338579-122338629	HCM	heart:	n/a
11	chr7:122339531-122339581	PANC-1	pancreas:	n/a
12	chr7:122338579-122338629	SK-N-SH	brain:	n/a
13	chr7:122340281-122340331	IMR90	lung:	fetal
14	chr7:122340193-122340243	PrEC	prostate:	n/a
15	chr7:122339531-122339581	A549	lung:	n/a
16	chr7:122338579-122338629	HEEpiC	esophagus:	n/a
17	chr7:122342889-122342939	AG04449	skin:	fetal
18	chr7:122342889-122342939	AG09319	gingival:	n/a
19	chr7:122339531-122339581	NHBE	bronchial:	n/a
20	chr7:122338985-122339035	HCPEpiC	choroid plexus:	n/a
21	chr7:122342889-122342939	AG10803	skin:	n/a
22	chr7:122340281-122340331	BJ	skin:	n/a
23	chr7:122343409-122343459	BJ	skin:	n/a
24	chr7:122338985-122339035	HCM	heart:	n/a
25	chr7:122339531-122339581	GM12892	blood:	n/a
26	chr7:122339531-122339581	HepG2	liver:	n/a
27	chr7:122342889-122342939	HPAEpiC	pulmonary alveolar:	n/a
28	chr7:122343409-122343459	NHBE	bronchial:	n/a
29	chr7:122338985-122339035	HRE	kidney:	n/a
30	chr7:122338985-122339035	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:122339531-122339581	HAEpiC	amniotic membrane:	n/a
32	chr7:122340193-122340243	MCF-7	breast:	n/a
33	chr7:122343409-122343459	PFSK-1	brain:	n/a
34	chr7:122338579-122338629	MCF10A-Er-Src	breast:	n/a
35	chr7:122338579-122338629	A549	lung:	n/a
36	chr7:122340193-122340243	HAEpiC	amniotic membrane:	n/a
37	chr7:122326807-122326857	CMK	blood:	n/a
38	chr7:122342889-122342939	BE2_C	brain:	n/a
39	chr7:122343409-122343459	GM12892	blood:	n/a
40	chr7:122340193-122340243	ProgFib	skin:	n/a
41	chr7:122338579-122338629	NB4	blood:	n/a
42	chr7:122338985-122339035	H1-hESC	embryonic stem cell:	embryo
43	chr7:122339531-122339581	HNPCEpiC	eye:	n/a
44	chr7:122339531-122339581	NT2-D1	testis:	n/a
45	chr7:122326807-122326857	Jurkat	blood:	n/a
46	chr7:122343409-122343459	MCF10A-Er-Src	breast:	n/a
47	chr7:122340193-122340243	RPTEC	kidney:	n/a
48	chr7:122340281-122340331	Hela-S3	cervix:	n/a
49	chr7:122342889-122342939	K562	blood:	n/a
50	chr7:122342889-122342939	AoSMC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:122333145..122337582-chr7:122337646..122340528,4	K562	blood:
2	chr7:122368871..122371613-chr7:122375877..122379228,3	MCF-7	breast:
3	chr7:122337511..122339668-chr7:122352052..122353795,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNF148	TF binding region
RNF133	TF binding region
RNF148	CpG island
RNF133	CpG island
ENSG00000188050	chromatin interactions

Extended variants
information (count: 2038 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:2038 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540487146	chr7:122325874-122325875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs140377786	chr7:122325881-122325882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs150381087	chr7:122325889-122325890	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545461654	chr7:122325951-122325952	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs546759277	chr7:122325969-122325970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531425282	chr7:122326071-122326072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs577180166	chr7:122326076-122326077	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186012490	chr7:122326130-122326131	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs561818822	chr7:122326146-122326147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138013777	chr7:122326150-122326151	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs190639469	chr7:122326210-122326211	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs566773363	chr7:122326224-122326225	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs62482259	chr7:122326258-122326259	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539050568	chr7:122326289-122326290	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs142174263	chr7:122326305-122326306	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528266535	chr7:122326350-122326351	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs569047594	chr7:122326409-122326410	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77082944	chr7:122326462-122326463	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553414433	chr7:122326466-122326467	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs574670743	chr7:122326565-122326566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs146057378	chr7:122326571-122326572	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs67765659	chr7:122326613-122326614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs574660380	chr7:122326619-122326620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs138385796	chr7:122326640-122326641	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554478870	chr7:122326658-122326659	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577453149	chr7:122326676-122326677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545826401	chr7:122326785-122326786	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556192288	chr7:122326790-122326791	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576209126	chr7:122326797-122326798	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs67203312	chr7:122326800-122326801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541905300	chr7:122326808-122326809	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561879777	chr7:122326832-122326833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs567249205	chr7:122326864-122326865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527452721	chr7:122326880-122326881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs143931943	chr7:122326899-122326900	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147239954	chr7:122326928-122326929	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs56029822	chr7:122326962-122326963	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552585983	chr7:122326991-122326992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568874651	chr7:122327017-122327018	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560136191	chr7:122327052-122327053	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531710261	chr7:122327085-122327086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552782424	chr7:122327117-122327118	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs548251197	chr7:122327152-122327153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs568196993	chr7:122327174-122327175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs80236888	chr7:122327176-122327177	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554064976	chr7:122327177-122327178	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183291974	chr7:122327184-122327185	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186200522	chr7:122327209-122327210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369055214	chr7:122327311-122327312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141556594	chr7:122327328-122327329	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
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
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
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	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	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Acute monocytic leukemia	16498392	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:182 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:122317600-122326600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr7:122317600-122327000	Weak transcription	Fetal Stomach	stomach
3	chr7:122320400-122326400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:122320800-122329400	Weak transcription	Fetal Intestine Small	intestine
5	chr7:122322400-122329200	Weak transcription	Gastric	stomach
6	chr7:122322600-122328400	Weak transcription	HepG2	liver
7	chr7:122323200-122328600	Weak transcription	Pancreas	Pancrea
8	chr7:122324000-122326600	Weak transcription	Left Ventricle	heart
9	chr7:122324000-122331600	Weak transcription	Lung	lung
10	chr7:122324000-122336000	Weak transcription	Right Atrium	heart
11	chr7:122324200-122336000	Weak transcription	Fetal Lung	lung
12	chr7:122325200-122326000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr7:122325200-122327600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr7:122325200-122327600	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr7:122325200-122327600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr7:122325200-122327600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr7:122325200-122327800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr7:122325200-122327800	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr7:122325200-122327800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:122325200-122329000	Enhancers	Fetal Heart	heart
21	chr7:122325600-122328400	Weak transcription	Stomach Mucosa	stomach
22	chr7:122325600-122329600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr7:122325800-122326600	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr7:122325800-122327000	Weak transcription	Placenta Amnion	Placenta Amnion
25	chr7:122326000-122326400	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr7:122326400-122327600	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr7:122326400-122327600	Enhancers	H1 Cell Line	embryonic stem cell
28	chr7:122326600-122327000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr7:122326600-122327000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr7:122326600-122327000	Enhancers	Fetal Muscle Leg	muscle
31	chr7:122326600-122327000	Enhancers	Left Ventricle	heart
32	chr7:122326600-122327600	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr7:122326800-122327000	Enhancers	Fetal Muscle Trunk	muscle
34	chr7:122327000-122327600	Enhancers	Placenta Amnion	Placenta Amnion
35	chr7:122327000-122328400	Weak transcription	Fetal Muscle Leg	muscle
36	chr7:122327000-122328400	Weak transcription	Left Ventricle	heart
37	chr7:122327000-122329600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr7:122327600-122328600	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr7:122327600-122329600	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr7:122327600-122332200	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr7:122327600-122332600	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr7:122327600-122336000	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr7:122327800-122332200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
44	chr7:122328200-122328400	Bivalent Enhancer	HSMMtube	muscle
45	chr7:122328400-122329200	Enhancers	HSMMtube	muscle
46	chr7:122328400-122329400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr7:122328400-122329400	Enhancers	Fetal Muscle Leg	muscle
48	chr7:122328400-122330000	Enhancers	Stomach Mucosa	stomach
49	chr7:122328400-122330200	Enhancers	Left Ventricle	heart
50	chr7:122328400-122330400	Enhancers	HepG2	liver

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