Variant report

Variant	nsv889238
Chromosome Location	chr7:136915059-136989606
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:225)
CpG islands
(count:368)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:225 , 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	CEBPB	chr7:136945439-136945666	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr7:136915386-136915658	HepG2	liver:	n/a	n/a
3	CEBPB	chr7:136928509-136928742	HepG2	liver:	n/a	n/a
4	CEBPB	chr7:136918947-136919088	HepG2	liver:	n/a	chr7:136919023-136919034
5	CEBPB	chr7:136947739-136947900	IMR90	lung:	n/a	n/a
6	CEBPB	chr7:136915432-136915693	IMR90	lung:	n/a	n/a
7	CEBPB	chr7:136915475-136915645	A549	lung:	n/a	n/a
8	CEBPB	chr7:136956417-136956716	HepG2	liver:	n/a	chr7:136956559-136956570
9	CTCF	chr7:136922260-136922410	K562	blood:	n/a	n/a
10	CTCF	chr7:136972500-136972650	HCPEpiC	choroid plexus:	n/a	n/a
11	CTCF	chr7:136972440-136972590	AG09309	skin:	n/a	n/a
12	CTCF	chr7:136972453-136972644	SK-N-SH_RA	brain:	n/a	n/a
13	CTCF	chr7:136972520-136972670	RPTEC	kidney:	n/a	n/a
14	CTCF	chr7:136972480-136972630	BJ	skin:	n/a	n/a
15	CTCF	chr7:136972580-136972730	HEEpiC	esophagus:	n/a	n/a
16	CTCF	chr7:136972540-136972690	HEK293	kidney:	n/a	n/a
17	CTCF	chr7:136972440-136972590	HFF-Myc	foreskin:	n/a	n/a
18	CTCF	chr7:136972460-136972610	GM12864	blood:	n/a	n/a
19	CTCF	chr7:136989600-136989750	BJ	skin:	n/a	n/a
20	CTCF	chr7:136989420-136989570	HA-sp	spinal cord:	n/a	n/a
21	CTCF	chr7:136972540-136972790	GM12874	blood:	n/a	n/a
22	CTCF	chr7:136972460-136972610	HCT-116	colon:	n/a	n/a
23	CTCF	chr7:136984100-136984250	GM06990	blood:	n/a	n/a
24	CTCF	chr7:136989340-136989490	HAc	cerebellar:	n/a	n/a
25	CTCF	chr7:136972460-136972610	GM12865	blood:	n/a	n/a
26	CTCF	chr7:136972520-136972670	HMEC	breast:	n/a	n/a
27	CTCF	chr7:136972520-136972670	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr7:136972520-136972670	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr7:136989520-136989670	HBMEC	blood vessel:	n/a	n/a
30	CTCF	chr7:136926580-136926730	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr7:136972540-136972690	GM06990	blood:	n/a	n/a
32	CTCF	chr7:136972440-136972590	HCFaa	heart:	n/a	n/a
33	CTCF	chr7:136972500-136972650	NHEK	skin:	n/a	n/a
34	CTCF	chr7:136972480-136972630	K562	blood:	n/a	n/a
35	CTCF	chr7:136965100-136965250	MCF-7	breast:	n/a	n/a
36	CTCF	chr7:136989500-136989650	HPAF	blood vessel:	n/a	n/a
37	CTCF	chr7:136972580-136972730	HVMF	connective:	n/a	n/a
38	CTCF	chr7:136972520-136972670	HRE	kidney:	n/a	n/a
39	CTCF	chr7:136972559-136972625	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr7:136972520-136972670	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr7:136972460-136972610	HCM	heart:	n/a	n/a
42	CTCF	chr7:136989440-136989590	BE2_C	brain:	n/a	n/a
43	CTCF	chr7:136972560-136972710	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:136972560-136972710	MCF-7	breast:	n/a	n/a
45	CTCF	chr7:136972600-136972750	GM12875	blood:	n/a	n/a
46	CTCF	chr7:136989480-136989630	AG04450	lung:	n/a	n/a
47	CTCF	chr7:136972480-136972630	RPTEC	kidney:	n/a	n/a
48	CTCF	chr7:136949778-136949828	GM13976	blood:	n/a	n/a
49	CTCF	chr7:136972520-136972670	AG10803	skin:	n/a	n/a
50	CTCF	chr7:136972404-136972761	IMR90	lung:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:136928644-136928694	CMK	blood:	n/a
2	chr7:136928644-136928694	HCT-116	colon:	n/a
3	chr7:136928644-136928694	CMK	blood:	n/a
4	chr7:136928644-136928694	HCT-116	colon:	n/a
5	chr7:136973838-136973888	SAEC	small airway:	n/a
6	chr7:136953057-136953107	ProgFib	skin:	n/a
7	chr7:136928644-136928694	SK-N-SH_RA	brain:	n/a
8	chr7:136927099-136927149	ovcar-3	ovarian:	n/a
9	chr7:136973838-136973888	HCM	heart:	n/a
10	chr7:136928644-136928694	SK-N-SH	brain:	n/a
11	chr7:136953057-136953107	HRCEpiC	kidney:	n/a
12	chr7:136944526-136944576	HCPEpiC	choroid plexus:	n/a
13	chr7:136928644-136928694	HMEC	breast:	n/a
14	chr7:136953057-136953107	T-47D	breast:	n/a
15	chr7:136927099-136927149	ECC-1	luminal epithelium:	n/a
16	chr7:136928644-136928694	HCF	heart:	n/a
17	chr7:136927099-136927149	SK-N-SH	brain:	n/a
18	chr7:136960138-136960188	ovcar-3	ovarian:	n/a
19	chr7:136927099-136927149	GM12892	blood:	n/a
20	chr7:136928644-136928694	AG04450	lung:	fetal
21	chr7:136953057-136953107	AG09309	skin:	n/a
22	chr7:136973838-136973888	GM19239	blood:	n/a
23	chr7:136960138-136960188	HCPEpiC	choroid plexus:	n/a
24	chr7:136944526-136944576	HEEpiC	esophagus:	n/a
25	chr7:136944526-136944576	GM19239	blood:	n/a
26	chr7:136944526-136944576	SK-N-SH_RA	brain:	n/a
27	chr7:136960138-136960188	GM12891	blood:	n/a
28	chr7:136928644-136928694	HRPEpiC	eye:	n/a
29	chr7:136973838-136973888	GM06990	blood:	n/a
30	chr7:136928644-136928694	NHBE	bronchial:	n/a
31	chr7:136944526-136944576	HEK293	kidney:	embryo
32	chr7:136944526-136944576	Jurkat	blood:	n/a
33	chr7:136928644-136928694	HEEpiC	esophagus:	n/a
34	chr7:136953057-136953107	MCF10A-Er-Src	breast:	n/a
35	chr7:136973838-136973888	HMEC	breast:	n/a
36	chr7:136973838-136973888	HRCEpiC	kidney:	n/a
37	chr7:136928644-136928694	AG04449	skin:	fetal
38	chr7:136944526-136944576	GM12878	blood:	n/a
39	chr7:136953057-136953107	HCM	heart:	n/a
40	chr7:136953057-136953107	HEK293	kidney:	embryo
41	chr7:136927099-136927149	SK-N-SH_RA	brain:	n/a
42	chr7:136960138-136960188	AG09309	skin:	n/a
43	chr7:136973838-136973888	HAEpiC	amniotic membrane:	n/a
44	chr7:136953057-136953107	AG10803	skin:	n/a
45	chr7:136953057-136953107	NHDF-neo	bronchial:	n/a
46	chr7:136928644-136928694	AG10803	skin:	n/a
47	chr7:136953057-136953107	AG04450	lung:	fetal
48	chr7:136973838-136973888	GM12892	blood:	n/a
49	chr7:136960138-136960188	A549	lung:	n/a
50	chr7:136944526-136944576	U87	brain:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
2	chr7:136939425..136941087-chr7:136941192..136943070,2	K562	blood:
3	chr7:136939425..136941087-chr7:136941192..136943070,2	K562	blood:
4	chr12:62807018..62807608-chr7:136989360..136989935,2	MCF-7	breast:
5	chr7:136926388..136929879-chr7:136930158..136932908,3	K562	blood:
6	chr7:136926388..136928401-chr7:136930158..136932908,2	K562	blood:
7	chr7:136915740..136917893-chr7:136923118..136925670,2	K562	blood:
8	chr7:136926388..136928401-chr7:136930158..136932908,2	K562	blood:
9	chr7:136915442..136917934-chr7:136955995..136958425,2	K562	blood:
10	chr7:136930142..136933282-chr7:136935160..136937647,3	K562	blood:
11	chr7:136926388..136929879-chr7:136930158..136932908,3	K562	blood:
12	chr7:136915740..136917893-chr7:136923118..136925670,2	K562	blood:
13	chr7:136930142..136933282-chr7:136935160..136937647,3	K562	blood:
14	chr7:136960021..136961767-chr7:136965044..136967236,2	K562	blood:
15	chr7:136983518..136985110-chr7:136986061..136988614,2	MCF-7	breast:
16	chr7:136915442..136917934-chr7:136955995..136958425,2	K562	blood:
17	chr7:136960021..136961767-chr7:136965044..136967236,2	K562	blood:
18	chr7:136911465..136914095-chr7:136917447..136919624,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000202023	TF binding region
ENSG00000202023	CpG island

Extended variants
information (count: 2806 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2806 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17168990	chr7:136915059-136915060	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551463920	chr7:136915060-136915061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs145838125	chr7:136915065-136915066	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541372359	chr7:136915078-136915079	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185115226	chr7:136915084-136915085	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187964027	chr7:136915105-136915106	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369838013	chr7:136915175-136915176	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530460564	chr7:136915180-136915181	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374242597	chr7:136915190-136915191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544114645	chr7:136915230-136915231	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34913884	chr7:136915250-136915251	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs563902759	chr7:136915316-136915317	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11561959	chr7:136915362-136915363	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs182472989	chr7:136915383-136915384	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs369425967	chr7:136915393-136915394	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs1451528	chr7:136915408-136915409	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs148968829	chr7:136915462-136915463	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528078941	chr7:136915500-136915501	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548214554	chr7:136915535-136915536	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs567709067	chr7:136915545-136915546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567253178	chr7:136915549-136915550	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34263682	chr7:136915559-136915560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536982143	chr7:136915632-136915633	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374927156	chr7:136915657-136915658	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550437927	chr7:136915658-136915659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369073929	chr7:136915663-136915664	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187043296	chr7:136915665-136915666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532277931	chr7:136915730-136915731	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs558788854	chr7:136915745-136915746	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572453451	chr7:136915753-136915754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145699069	chr7:136915784-136915785	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs554984990	chr7:136915826-136915827	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs146565992	chr7:136915839-136915840	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs192215042	chr7:136915854-136915855	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181825758	chr7:136915869-136915870	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376395871	chr7:136915953-136915954	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555753961	chr7:136915995-136915996	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs73727897	chr7:136916053-136916054	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546332408	chr7:136916081-136916082	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559690055	chr7:136916110-136916111	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186074071	chr7:136916116-136916117	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs547960782	chr7:136916194-136916195	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs141238520	chr7:136916205-136916206	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs530395695	chr7:136916207-136916208	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs550475161	chr7:136916218-136916219	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs145013919	chr7:136916234-136916235	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539257618	chr7:136916306-136916307	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190396748	chr7:136916327-136916328	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs17168991	chr7:136916392-136916393	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs148297053	chr7:136916393-136916394	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	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
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Low-grade fibromyxoid sarcoma	21536545	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Neuroticism	17667963	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute myeloid leukemia	17237825	CNVD
Esophageal cancer	21851588	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:556 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136901600-136922800	Strong transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:136902000-136933800	Weak transcription	Fetal Brain Female	brain
3	chr7:136902200-136915800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:136906600-136925200	Weak transcription	Fetal Stomach	stomach
5	chr7:136909200-136922600	Weak transcription	Brain Hippocampus Middle	brain
6	chr7:136909600-136935800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:136909800-136926200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
8	chr7:136909800-136943000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr7:136911000-136922400	Weak transcription	Brain Substantia Nigra	brain
10	chr7:136911000-136927000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr7:136911200-136925800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:136911600-136936400	Weak transcription	Fetal Heart	heart
13	chr7:136911800-136920800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr7:136912400-136922800	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr7:136913400-136937200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr7:136913800-136918400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr7:136915000-136918600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr7:136915200-136935000	Weak transcription	Fetal Muscle Trunk	muscle
19	chr7:136915800-136917800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr7:136917200-136923800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:136917800-136922400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr7:136918400-136920400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr7:136918600-136922400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr7:136920000-136920200	Enhancers	Fetal Kidney	kidney
25	chr7:136920200-136939000	Weak transcription	Fetal Kidney	kidney
26	chr7:136920400-136921200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr7:136920800-136923000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
28	chr7:136921200-136924600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr7:136922400-136922600	Enhancers	Brain Substantia Nigra	brain
30	chr7:136922400-136923200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr7:136922400-136923200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:136922400-136935600	Weak transcription	Placenta	Placenta
33	chr7:136922600-136923000	Weak transcription	Brain Substantia Nigra	brain
34	chr7:136922600-136924000	Enhancers	Brain Hippocampus Middle	brain
35	chr7:136922800-136923000	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr7:136922800-136923200	Genic enhancers	Cortex derived primary cultured neurospheres	brain
37	chr7:136922800-136923800	Enhancers	Brain Cingulate Gyrus	brain
38	chr7:136923000-136923200	Enhancers	Brain Angular Gyrus	brain
39	chr7:136923000-136923200	Enhancers	Brain Substantia Nigra	brain
40	chr7:136923000-136926600	Weak transcription	Brain Inferior Temporal Lobe	brain
41	chr7:136923000-136928000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr7:136923200-136924000	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:136923200-136925400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr7:136923200-136926600	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr7:136923200-136939600	Weak transcription	Brain Angular Gyrus	brain
46	chr7:136923200-136940200	Weak transcription	Brain Substantia Nigra	brain
47	chr7:136923600-136924000	Enhancers	Brain Anterior Caudate	brain
48	chr7:136923600-136937800	Weak transcription	Brain Germinal Matrix	brain
49	chr7:136923800-136924000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr7:136923800-136937600	Weak transcription	Brain Cingulate Gyrus	brain

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