Variant report

Variant	nsv971048
Chromosome Location	chr7:128298277-128300276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:82)
CpG islands
(count:61)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:82 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:128298658-128298767	Lung_OC	lung:	n/a	n/a
2	FAM48A	chr7:128300191-128300305	GM12878	blood:	n/a	n/a
3	FOSL2	chr7:128298493-128299066	HepG2	liver:	n/a	n/a
4	FOSL2	chr7:128297970-128298431	HepG2	liver:	n/a	n/a
5	FOSL2	chr7:128299884-128300332	HepG2	liver:	n/a	n/a
6	FOSL2	chr7:128299156-128299778	HepG2	liver:	n/a	n/a
7	HEY1	chr7:128298550-128298940	HepG2	liver:	n/a	n/a
8	JUND	chr7:128298569-128298907	HepG2	liver:	n/a	n/a
9	JUND	chr7:128298745-128298916	HepG2	liver:	n/a	n/a
10	MAFK	chr7:128298567-128298777	HepG2	liver:	n/a	chr7:128298626-128298641
11	MAFK	chr7:128298525-128298776	HepG2	liver:	n/a	chr7:128298626-128298641
12	NFYB	chr7:128298590-128298716	K562	blood:	n/a	n/a
13	PBX3	chr7:128298555-128298720	GM12878	blood:	n/a	n/a
14	POLR2A	chr7:128298523-128298960	GM12878	blood:	n/a	n/a
15	POLR2A	chr7:128299431-128299572	Hela-S3	cervix:	n/a	n/a
16	POLR2A	chr7:128298731-128298973	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr7:128298608-128298945	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr7:128297382-128298407	GM12892	blood:	n/a	n/a
19	POLR2A	chr7:128300240-128300512	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr7:128298546-128298973	HepG2	liver:	n/a	n/a
21	POLR2A	chr7:128298552-128299003	GM12891	blood:	n/a	n/a
22	POLR2A	chr7:128299366-128299788	SK-N-MC	brain:	n/a	n/a
23	POLR2A	chr7:128299586-128299720	Hela-S3	cervix:	n/a	n/a
24	POLR2A	chr7:128300075-128300178	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr7:128299353-128299366	HUVEC	blood vessel:	n/a	n/a
26	POLR2A	chr7:128298504-128298924	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr7:128299960-128300447	HepG2	liver:	n/a	n/a
28	POLR2A	chr7:128299481-128299570	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr7:128299442-128299774	GM12878	blood:	n/a	n/a
30	POLR2A	chr7:128299985-128300372	A549	lung:	n/a	n/a
31	POLR2A	chr7:128298520-128298924	GM12878	blood:	n/a	n/a
32	POLR2A	chr7:128298489-128298983	K562	blood:	n/a	n/a
33	POLR2A	chr7:128298522-128299098	K562	blood:	n/a	n/a
34	POLR2A	chr7:128298454-128299102	GM12878	blood:	n/a	n/a
35	POLR2A	chr7:128298682-128298870	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr7:128300128-128300161	K562	blood:	n/a	n/a
37	POLR2A	chr7:128298492-128298847	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr7:128299496-128299811	GM12892	blood:	n/a	n/a
39	POLR2A	chr7:128298754-128298812	K562	blood:	n/a	n/a
40	POLR2A	chr7:128298474-128299025	GM12891	blood:	n/a	n/a
41	POLR2A	chr7:128297321-128298394	GM12878	blood:	n/a	n/a
42	POLR2A	chr7:128298029-128298397	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr7:128298527-128298924	GM12878	blood:	n/a	n/a
44	POLR2A	chr7:128300122-128300246	MCF-7	breast:	n/a	n/a
45	POLR2A	chr7:128299838-128300435	SK-N-SH	brain:	n/a	n/a
46	POLR2A	chr7:128298545-128299146	SK-N-MC	brain:	n/a	n/a
47	POLR2A	chr7:128299803-128299811	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr7:128299872-128300340	GM12878	blood:	n/a	n/a
49	POLR2A	chr7:128299296-128299741	HepG2	liver:	n/a	n/a
50	POLR2A	chr7:128299988-128300031	Hela-S3	cervix:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128300012-128300062	PANC-1	pancreas:	n/a
2	chr7:128300012-128300062	Hela-S3	cervix:	n/a
3	chr7:128300012-128300062	BE2_C	brain:	n/a
4	chr7:128300012-128300062	PFSK-1	brain:	n/a
5	chr7:128300012-128300062	HCT-116	colon:	n/a
6	chr7:128300012-128300062	ProgFib	skin:	n/a
7	chr7:128300012-128300062	AG09309	skin:	n/a
8	chr7:128300012-128300062	HL-60	blood:	n/a
9	chr7:128300012-128300062	AG04449	skin:	fetal
10	chr7:128300012-128300062	Caco-2	colon:	n/a
11	chr7:128300012-128300062	Hepatocyte	liver:	n/a
12	chr7:128300012-128300062	NB4	blood:	n/a
13	chr7:128300012-128300062	HPAEpiC	pulmonary alveolar:	n/a
14	chr7:128300012-128300062	K562	blood:	n/a
15	chr7:128300012-128300062	RPTEC	kidney:	n/a
16	chr7:128300012-128300062	GM12891	blood:	n/a
17	chr7:128300012-128300062	A549	lung:	n/a
18	chr7:128300012-128300062	HAEpiC	amniotic membrane:	n/a
19	chr7:128300012-128300062	HRCEpiC	kidney:	n/a
20	chr7:128300012-128300062	HepG2	liver:	n/a
21	chr7:128300012-128300062	IMR90	lung:	fetal
22	chr7:128300012-128300062	MCF10A-Er-Src	breast:	n/a
23	chr7:128300012-128300062	MCF-7	breast:	n/a
24	chr7:128300012-128300062	LNCaP	prostate:	n/a
25	chr7:128300012-128300062	T-47D	breast:	n/a
26	chr7:128300012-128300062	H1-hESC	embryonic stem cell:	embryo
27	chr7:128300012-128300062	HRPEpiC	eye:	n/a
28	chr7:128300012-128300062	NT2-D1	testis:	n/a
29	chr7:128300012-128300062	HIPEpiC	eye:	n/a
30	chr7:128300012-128300062	BJ	skin:	n/a
31	chr7:128300012-128300062	GM12892	blood:	n/a
32	chr7:128300012-128300062	HNPCEpiC	eye:	n/a
33	chr7:128300012-128300062	NHBE	bronchial:	n/a
34	chr7:128300012-128300062	SKMC	muscle:	n/a
35	chr7:128300012-128300062	GM12878	blood:	n/a
36	chr7:128300012-128300062	AoSMC	blood vessel:	n/a
37	chr7:128300012-128300062	HEK293	kidney:	embryo
38	chr7:128300012-128300062	AG09319	gingival:	n/a
39	chr7:128300012-128300062	NHDF-neo	bronchial:	n/a
40	chr7:128300012-128300062	HCPEpiC	choroid plexus:	n/a
41	chr7:128300012-128300062	CMK	blood:	n/a
42	chr7:128300012-128300062	HMEC	breast:	n/a
43	chr7:128300012-128300062	GM06990	blood:	n/a
44	chr7:128300012-128300062	ovcar-3	ovarian:	n/a
45	chr7:128300012-128300062	Jurkat	blood:	n/a
46	chr7:128300012-128300062	PrEC	prostate:	n/a
47	chr7:128300012-128300062	HUVEC	blood vessel:	n/a
48	chr7:128300012-128300062	NH-A	brain:	n/a
49	chr7:128300012-128300062	SK-N-SH_RA	brain:	n/a
50	chr7:128300012-128300062	ECC-1	luminal epithelium:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:128115173..128117389-chr7:128298817..128301721,2	K562	blood:
2	chr7:128298702..128300846-chr7:128378149..128381069,2	K562	blood:
3	chr7:128299231..128302133-chr7:128312144..128313833,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000229413	TF binding region
CICP14	TF binding region
ENSG00000229413	CpG island
CICP14	CpG island
ENSG00000165055	chromatin interactions
ENSG00000128595	chromatin interactions
ENSG00000205085	chromatin interactions

Extended variants
information (count: 85 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:85 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112913702	chr7:128298292-128298293	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs538692575	chr7:128298323-128298324	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs375729115	chr7:128298334-128298335	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs62481937	chr7:128298370-128298371	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs554068861	chr7:128298417-128298418	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs572530589	chr7:128298445-128298446	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs533350559	chr7:128298453-128298454	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542738782	chr7:128298472-128298473	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs552128920	chr7:128298541-128298542	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs73723614	chr7:128298600-128298601	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs199608151	chr7:128298609-128298610	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs148615684	chr7:128298645-128298646	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs544528341	chr7:128298661-128298662	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs189675160	chr7:128298665-128298666	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs142099051	chr7:128298668-128298669	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs545217730	chr7:128298679-128298680	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs374162277	chr7:128298703-128298704	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs560077277	chr7:128298736-128298737	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs34292188	chr7:128298745-128298746	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs181221850	chr7:128298767-128298768	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548638460	chr7:128298784-128298785	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs147798343	chr7:128298791-128298792	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531166679	chr7:128298792-128298793	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs549354982	chr7:128298806-128298807	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs373067532	chr7:128298808-128298809	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs538940837	chr7:128298813-128298814	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs554378774	chr7:128298814-128298815	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs186098340	chr7:128298863-128298864	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs1809083	chr7:128298881-128298882	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562292730	chr7:128298892-128298893	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs555060740	chr7:128298900-128298901	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs114191334	chr7:128298920-128298921	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	mRNA abundance
33	rs9719026	chr7:128298972-128298973	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs9718607	chr7:128298973-128298974	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs58211466	chr7:128298974-128298975	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs534090589	chr7:128298978-128298979	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs397796577	chr7:128298987-128298988	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs188126508	chr7:128298988-128298989	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs377365495	chr7:128299001-128299002	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs58163910	chr7:128299016-128299017	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs374062987	chr7:128299029-128299030	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs144813597	chr7:128299031-128299032	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs4728127	chr7:128299034-128299035	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs560320466	chr7:128299071-128299072	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs572096911	chr7:128299113-128299114	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs542320316	chr7:128299114-128299115	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs560687781	chr7:128299165-128299166	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs200743864	chr7:128299183-128299184	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs376016114	chr7:128299184-128299185	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs397945286	chr7:128299185-128299186	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
Endometrioid adenocarcinoma	16974079	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
Biliary cancer	19435499	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Melanoma	19188590	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Basal cell lymphoma	21115979	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Coffin-Siris syndrome	21572526	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Retinitis pigmentosa	17160897	CNVD
Colorblindness	17160897	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128249600-128308400	Weak transcription	HSMM	muscle
2	chr7:128249600-128312200	Weak transcription	Psoas Muscle	Psoas
3	chr7:128249600-128319600	Weak transcription	NHLF	lung
4	chr7:128260400-128300600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr7:128272200-128300000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:128279800-128300000	Weak transcription	Dnd41	blood
7	chr7:128279800-128301400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
8	chr7:128282400-128301400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr7:128282400-128312400	Weak transcription	Skeletal Muscle Female	skeletal muscle
10	chr7:128282600-128300000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:128284000-128304800	Weak transcription	Primary T cells from cord blood	blood
12	chr7:128284200-128301400	Weak transcription	Fetal Lung	lung
13	chr7:128284200-128313200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr7:128284400-128299200	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr7:128284400-128313200	Weak transcription	Colon Smooth Muscle	Colon
16	chr7:128286400-128298400	Weak transcription	Monocytes-CD14+_RO01746	blood
17	chr7:128287400-128301400	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr7:128289000-128301400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr7:128292000-128300000	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr7:128292200-128300000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr7:128293000-128300000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr7:128293400-128300200	Weak transcription	Brain Anterior Caudate	brain
23	chr7:128293600-128301400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr7:128293600-128301600	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr7:128293600-128302000	Weak transcription	Stomach Smooth Muscle	stomach
26	chr7:128293600-128302200	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr7:128293600-128312200	Weak transcription	Fetal Muscle Trunk	muscle
28	chr7:128294000-128301000	Weak transcription	Esophagus	oesophagus
29	chr7:128294000-128313200	Weak transcription	Brain Germinal Matrix	brain
30	chr7:128294200-128300000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr7:128294400-128302200	Weak transcription	Aorta	Aorta
32	chr7:128294600-128301400	Weak transcription	Spleen	Spleen
33	chr7:128294600-128301800	Weak transcription	Fetal Brain Female	brain
34	chr7:128294800-128301000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr7:128294800-128301400	Weak transcription	Fetal Muscle Leg	muscle
36	chr7:128294800-128302200	Weak transcription	Gastric	stomach
37	chr7:128294800-128328000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr7:128295000-128298400	Weak transcription	Adipose Nuclei	Adipose
39	chr7:128295000-128298600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr7:128295000-128298600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr7:128295000-128298600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr7:128295000-128300000	Weak transcription	Fetal Thymus	thymus
43	chr7:128295000-128300000	Weak transcription	Lung	lung
44	chr7:128295000-128300800	Weak transcription	Placenta	Placenta
45	chr7:128295000-128301200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:128295000-128301400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr7:128295000-128301400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr7:128295000-128301400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:128295000-128301400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
50	chr7:128295000-128301600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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