Variant report

Variant	nsv970938
Chromosome Location	chr7:128256300-128300276
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:398)
CpG islands
(count:611)
Chromatin interactive
region (count:3)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:128286190-128286509	GM12878	blood:	n/a	n/a
2	CBX3	chr7:128270470-128270792	K562	blood:	n/a	n/a
3	CBX3	chr7:128293288-128293860	K562	blood:	n/a	n/a
4	CBX3	chr7:128291764-128292046	K562	blood:	n/a	n/a
5	CEBPB	chr7:128293514-128293858	K562	blood:	n/a	n/a
6	CEBPB	chr7:128293555-128293810	K562	blood:	n/a	n/a
7	CTCF	chr7:128293106-128293632	K562	blood:	n/a	n/a
8	CTCF	chr7:128291880-128292030	GM12872	blood:	n/a	n/a
9	CTCF	chr7:128291593-128292126	K562	blood:	n/a	n/a
10	CTCF	chr7:128295220-128295370	RPTEC	kidney:	n/a	n/a
11	CTCF	chr7:128291759-128292043	A549	lung:	n/a	n/a
12	CTCF	chr7:128291903-128292005	GM12891	blood:	n/a	n/a
13	CTCF	chr7:128291913-128291985	GM12878	blood:	n/a	n/a
14	CTCF	chr7:128291880-128292030	MCF-7	breast:	n/a	n/a
15	CTCF	chr7:128291907-128291988	Gliobla	brain:	n/a	n/a
16	CTCF	chr7:128290448-128290814	K562	blood:	n/a	n/a
17	CTCF	chr7:128291820-128291970	GM12872	blood:	n/a	n/a
18	CTCF	chr7:128291860-128292010	HFF	foreskin:	n/a	n/a
19	CTCF	chr7:128291880-128292030	NHDF-neo	bronchial:	n/a	n/a
20	CTCF	chr7:128293260-128293410	HBMEC	blood vessel:	n/a	n/a
21	CTCF	chr7:128291924-128291983	GM12892	blood:	n/a	n/a
22	CTCF	chr7:128291900-128292050	SAEC	small airway:	n/a	n/a
23	CTCF	chr7:128291810-128292061	K562	blood:	n/a	n/a
24	CTCF	chr7:128295220-128295370	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr7:128291840-128291990	HEK293	kidney:	n/a	n/a
26	CTCF	chr7:128291840-128291990	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr7:128291913-128292015	GM19240	blood:	n/a	n/a
28	CTCF	chr7:128280980-128281130	GM12875	blood:	n/a	n/a
29	CTCF	chr7:128291900-128292050	SK-N-SH_RA	brain:	n/a	n/a
30	CTCF	chr7:128295200-128295350	HCT-116	colon:	n/a	n/a
31	CTCF	chr7:128295344-128295412	H1-hESC	embryonic stem cell:	n/a	chr7:128295374-128295387
32	CTCF	chr7:128291867-128291983	HepG2	liver:	n/a	n/a
33	CTCF	chr7:128293320-128293470	GM12868	blood:	n/a	n/a
34	CTCF	chr7:128291424-128292223	K562	blood:	n/a	n/a
35	CTCF	chr7:128293280-128293430	K562	blood:	n/a	n/a
36	CTCF	chr7:128291921-128291994	GM19238	blood:	n/a	n/a
37	CTCF	chr7:128291840-128291990	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr7:128295220-128295370	HEK293	kidney:	n/a	n/a
39	CTCF	chr7:128291860-128292010	BE2_C	brain:	n/a	n/a
40	CTCF	chr7:128291938-128291953	MCF-7	breast:	n/a	n/a
41	CTCF	chr7:128290760-128290910	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr7:128290498-128290876	K562	blood:	n/a	n/a
43	CTCF	chr7:128263240-128263390	K562	blood:	n/a	n/a
44	CTCF	chr7:128295220-128295370	Hela-S3	cervix:	n/a	n/a
45	CTCF	chr7:128291880-128292030	AG04449	skin:	n/a	n/a
46	CTCF	chr7:128291840-128291990	AG09319	gingival:	n/a	n/a
47	CTCF	chr7:128295220-128295370	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr7:128293360-128293510	RPTEC	kidney:	n/a	n/a
49	CTCF	chr7:128291840-128291990	GM12874	blood:	n/a	n/a
50	CTCF	chr7:128295200-128295350	GM12866	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:128294794-128294844	K562	blood:	n/a
2	chr7:128294794-128294844	K562	blood:	n/a
3	chr7:128294083-128294133	HAEpiC	amniotic membrane:	n/a
4	chr7:128293756-128293806	GM06990	blood:	n/a
5	chr7:128292968-128293018	SKMC	muscle:	n/a
6	chr7:128294794-128294844	SK-N-SH	brain:	n/a
7	chr7:128292968-128293018	A549	lung:	n/a
8	chr7:128293588-128293638	T-47D	breast:	n/a
9	chr7:128280387-128280437	T-47D	breast:	n/a
10	chr7:128300012-128300062	HepG2	liver:	n/a
11	chr7:128294794-128294844	HepG2	liver:	n/a
12	chr7:128280248-128280298	GM12891	blood:	n/a
13	chr7:128300012-128300062	IMR90	lung:	fetal
14	chr7:128293756-128293806	GM12892	blood:	n/a
15	chr7:128293588-128293638	HCT-116	colon:	n/a
16	chr7:128293756-128293806	BE2_C	brain:	n/a
17	chr7:128294405-128294455	AG04449	skin:	fetal
18	chr7:128280279-128280329	U87	brain:	n/a
19	chr7:128280279-128280329	NHBE	bronchial:	n/a
20	chr7:128293756-128293806	HUVEC	blood vessel:	n/a
21	chr7:128293588-128293638	ProgFib	skin:	n/a
22	chr7:128293588-128293638	NH-A	brain:	n/a
23	chr7:128294083-128294133	GM12892	blood:	n/a
24	chr7:128294794-128294844	ovcar-3	ovarian:	n/a
25	chr7:128294405-128294455	SK-N-MC	brain:	n/a
26	chr7:128280248-128280298	GM06990	blood:	n/a
27	chr7:128292968-128293018	GM12891	blood:	n/a
28	chr7:128294405-128294455	ECC-1	luminal epithelium:	n/a
29	chr7:128293588-128293638	HCPEpiC	choroid plexus:	n/a
30	chr7:128294405-128294455	GM12892	blood:	n/a
31	chr7:128292968-128293018	BJ	skin:	n/a
32	chr7:128293588-128293638	HCF	heart:	n/a
33	chr7:128294083-128294133	CMK	blood:	n/a
34	chr7:128280248-128280298	HUVEC	blood vessel:	n/a
35	chr7:128280279-128280329	A549	lung:	n/a
36	chr7:128280248-128280298	HL-60	blood:	n/a
37	chr7:128292968-128293018	AG09319	gingival:	n/a
38	chr7:128280387-128280437	ECC-1	luminal epithelium:	n/a
39	chr7:128280387-128280437	GM12892	blood:	n/a
40	chr7:128294405-128294455	HEEpiC	esophagus:	n/a
41	chr7:128294405-128294455	HL-60	blood:	n/a
42	chr7:128280248-128280298	LNCaP	prostate:	n/a
43	chr7:128293756-128293806	PrEC	prostate:	n/a
44	chr7:128280387-128280437	HEK293	kidney:	embryo
45	chr7:128300012-128300062	AoSMC	blood vessel:	n/a
46	chr7:128293756-128293806	HRPEpiC	eye:	n/a
47	chr7:128280387-128280437	NHDF-neo	bronchial:	n/a
48	chr7:128294794-128294844	NT2-D1	testis:	n/a
49	chr7:128294794-128294844	SK-N-SH_RA	brain:	n/a
50	chr7:128294794-128294844	PANC-1	pancreas:	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	chr7:128299231..128302133-chr7:128312144..128313833,2	K562	blood:
3	chr7:128298702..128300846-chr7:128378149..128381069,2	K562	blood:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71F2-1	chr7:128278998-128280471	NONHSAT123216
2	lnc-FAM71F2-1	chr7:128287990-128288095	NONHSAT123222
3	lnc-FAM71F2-1	chr7:128280776-128281433	NONHSAT123218
4	lnc-FAM71F2-1	chr7:128288846-128288927	NONHSAT123221
5	lnc-FAM71F2-1	chr7:128282271-128282330	NONHSAT123221
6	lnc-FAM71F2-1	chr7:128281386-128281433	NONHSAT123221
7	lnc-FAM71F2-1	chr7:128280784-128281433	NONHSAT123219
8	lnc-FAM71F2-1	chr7:128291092-128291134	NONHSAT123222
9	lnc-FAM71F2-1	chr7:128278828-128281168	XLOC_006242
10	lnc-FAM71F2-1	chr7:128273086-128273159	NONHSAT123216
11	lnc-FAM71F2-1	chr7:128278644-128281373	NONHSAT123217
12	lnc-FAM71F2-1	chr7:128291092-128291151	NONHSAT123221
13	lnc-FAM71F2-1	chr7:128288840-128289065	NONHSAT123217
14	lnc-FAM71F2-1	chr7:128288960-128289038	NONHSAT123221
15	lnc-FAM71F2-1	chr7:128273069-128273159	XLOC_006242
16	lnc-FAM71F2-1	chr7:128281901-128282358	NONHSAT123217
17	lnc-FAM71F2-1	chr7:128291243-128291452	NONHSAT123221
18	lnc-FAM71F2-1	chr7:128291239-128292388	NONHSAT123224
19	lnc-FAM71F2-1	chr7:128282271-128282335	NONHSAT123218
20	lnc-FAM71F2-1	chr7:128288846-128289036	NONHSAT123222
21	lnc-FAM71F2-1	chr7:128288846-128289174	NONHSAT123218
22	lnc-FAM71F2-1	chr7:128282271-128282639	NONHSAT123219

No data

Variant related genes	Relation type
ENSG00000243679	TF binding region
ENSG00000229413	TF binding region
CICP14	TF binding region
RNU6-177P	TF binding region
ENSG00000230715	TF binding region
ENSG00000243302	TF binding region
ENSG00000243679	CpG island
ENSG00000229413	CpG island
CICP14	CpG island
RNU6-177P	CpG island
ENSG00000230715	CpG island
ENSG00000243302	CpG island
ENSG00000128595	chromatin interactions
ENSG00000165055	chromatin interactions
ENSG00000205085	chromatin interactions
KIF23	miRNA target sites
KIF26A	miRNA target sites

Extended variants
information (count: 1623 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1623 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537092822	chr7:128256308-128256309	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558872142	chr7:128256318-128256319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571569038	chr7:128256325-128256326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs183470742	chr7:128256345-128256346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs146236291	chr7:128256363-128256364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs554091165	chr7:128256375-128256376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139340311	chr7:128256464-128256465	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs34536793	chr7:128256492-128256493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs188014451	chr7:128256519-128256520	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs75178431	chr7:128256571-128256572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs75908671	chr7:128256572-128256573	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs554381588	chr7:128256573-128256574	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs112942470	chr7:128256585-128256586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs192847403	chr7:128256631-128256632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs556440713	chr7:128256634-128256635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564939598	chr7:128256649-128256650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs531973577	chr7:128256691-128256692	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78096410	chr7:128256720-128256721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs397741369	chr7:128256733-128256734	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs541361476	chr7:128256781-128256782	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs559600412	chr7:128256788-128256789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs530254911	chr7:128256803-128256804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144131013	chr7:128256818-128256819	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs146036082	chr7:128256841-128256842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs530987929	chr7:128256853-128256854	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs552387967	chr7:128256903-128256904	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs200540133	chr7:128256909-128256910	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534993767	chr7:128256930-128256931	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs554129981	chr7:128256949-128256950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542299901	chr7:128256953-128256954	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs148598709	chr7:128256959-128256960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs536065274	chr7:128256964-128256965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182662776	chr7:128256973-128256974	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576152829	chr7:128256988-128256989	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs142065258	chr7:128256990-128256991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs186706066	chr7:128257001-128257002	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558355531	chr7:128257006-128257007	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576461145	chr7:128257014-128257015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540599435	chr7:128257024-128257025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559636413	chr7:128257034-128257035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs369803420	chr7:128257039-128257040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192625868	chr7:128257062-128257063	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542062909	chr7:128257161-128257162	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184889989	chr7:128257164-128257165	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6467201	chr7:128257170-128257171	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs189270304	chr7:128257291-128257292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs62481873	chr7:128257292-128257293	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs530710680	chr7:128257300-128257301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs35638763	chr7:128257346-128257347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs6978360	chr7:128257350-128257351	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:81)

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
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:973 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:128200000-128258800	Weak transcription	Right Ventricle	heart
2	chr7:128204800-128258800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:128223800-128258800	Weak transcription	Lung	lung
4	chr7:128226400-128258800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:128233200-128258800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr7:128233200-128258800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr7:128233400-128258400	Weak transcription	Thymus	Thymus
8	chr7:128233400-128258600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:128233400-128258800	Weak transcription	Aorta	Aorta
10	chr7:128233400-128258800	Weak transcription	Esophagus	oesophagus
11	chr7:128233400-128258800	Weak transcription	Spleen	Spleen
12	chr7:128233400-128259000	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr7:128233400-128259000	Weak transcription	Colon Smooth Muscle	Colon
14	chr7:128233400-128259600	Weak transcription	Placenta Amnion	Placenta Amnion
15	chr7:128233400-128272000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr7:128233600-128258800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr7:128233800-128257600	Weak transcription	Primary hematopoietic stem cells	blood
18	chr7:128233800-128258800	Weak transcription	Fetal Brain Female	brain
19	chr7:128234600-128257600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr7:128234600-128258800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr7:128234600-128258800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr7:128234600-128258800	Weak transcription	Gastric	stomach
23	chr7:128234600-128271200	Weak transcription	Fetal Lung	lung
24	chr7:128235600-128258800	Weak transcription	Pancreas	Pancrea
25	chr7:128237600-128256600	Weak transcription	Fetal Muscle Leg	muscle
26	chr7:128237600-128258600	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr7:128237800-128290400	Weak transcription	HepG2	liver
28	chr7:128238200-128258800	Weak transcription	Ovary	ovary
29	chr7:128239200-128287200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr7:128239200-128296400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr7:128239400-128258800	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr7:128239400-128271200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr7:128239600-128258800	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr7:128239600-128262400	Weak transcription	Brain Hippocampus Middle	brain
35	chr7:128239800-128257600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr7:128239800-128258800	Weak transcription	Brain Cingulate Gyrus	brain
37	chr7:128240000-128258800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr7:128240200-128269400	Weak transcription	Primary B cells from cord blood	blood
39	chr7:128240400-128258800	Weak transcription	Primary T cells from cord blood	blood
40	chr7:128242600-128292800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr7:128246600-128284800	Weak transcription	Stomach Mucosa	stomach
42	chr7:128247000-128258800	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr7:128249600-128256800	Strong transcription	Dnd41	blood
44	chr7:128249600-128256800	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr7:128249600-128257200	Weak transcription	GM12878-XiMat	blood
46	chr7:128249600-128257600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr7:128249600-128257600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr7:128249600-128257800	Weak transcription	Rectal Mucosa Donor 31	rectum
49	chr7:128249600-128257800	Weak transcription	HMEC	breast
50	chr7:128249600-128257800	Weak transcription	K562	blood

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