Variant report

Variant	nsv508693
Chromosome Location	chr1:213406220-213421626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:213418013-213418264	K562	blood:	n/a	n/a
2	BACH1	chr1:213419375-213419497	K562	blood:	n/a	n/a
3	BHLHE40	chr1:213412214-213412215	K562	blood:	n/a	n/a
4	BHLHE40	chr1:213418029-213418347	HepG2	liver:	n/a	n/a
5	CHD1	chr1:213418540-213418566	GM12878	blood:	n/a	n/a
6	CTCF	chr1:213417716-213418508	A549	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
7	CTCF	chr1:213418374-213418435	GM12878	blood:	n/a	n/a
8	CTCF	chr1:213418080-213418230	HCPEpiC	choroid plexus:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
9	CTCF	chr1:213418060-213418210	HVMF	connective:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
10	CTCF	chr1:213418080-213418230	NB4	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
11	CTCF	chr1:213417680-213418469	SK-N-SH	brain:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
12	CTCF	chr1:213418020-213418170	HRE	kidney:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
13	CTCF	chr1:213418080-213418230	GM12867	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
14	CTCF	chr1:213418040-213418190	NHLF	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
15	CTCF	chr1:213417972-213418293	Medullo	brain:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
16	CTCF	chr1:213418029-213418232	HepG2	liver:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
17	CTCF	chr1:213418020-213418170	HCM	heart:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
18	CTCF	chr1:213418140-213418290	GM12866	blood:	n/a	n/a
19	CTCF	chr1:213417976-213418289	HCT-116	colon:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
20	CTCF	chr1:213418040-213418190	SK-N-SH_RA	brain:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
21	CTCF	chr1:213418060-213418210	Hela-S3	cervix:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
22	CTCF	chr1:213418040-213418190	HA-sp	spinal cord:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
23	CTCF	chr1:213417847-213418296	MCF-7	breast:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
24	CTCF	chr1:213418080-213418230	GM12873	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
25	CTCF	chr1:213418080-213418230	GM12872	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
26	CTCF	chr1:213418040-213418190	GM12865	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
27	CTCF	chr1:213417924-213418341	A549	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
28	CTCF	chr1:213418054-213418229	ProgFib	skin:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
29	CTCF	chr1:213418087-213418206	NHEK	skin:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
30	CTCF	chr1:213418040-213418190	HMF	breast:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
31	CTCF	chr1:213418109-213418197	GM19240	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
32	CTCF	chr1:213418040-213418190	BE2_C	brain:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
33	CTCF	chr1:213418080-213418230	GM12875	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
34	CTCF	chr1:213418024-213418196	GM13976	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
35	CTCF	chr1:213418000-213418150	HPF	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
36	CTCF	chr1:213418080-213418230	RPTEC	kidney:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
37	CTCF	chr1:213418040-213418190	HRPEpiC	eye:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
38	CTCF	chr1:213418160-213418310	WI-38	lung:	n/a	n/a
39	CTCF	chr1:213418040-213418190	HPF	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
40	CTCF	chr1:213418000-213418150	GM12871	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
41	CTCF	chr1:213418040-213418190	GM12878	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
42	CTCF	chr1:213418044-213418278	A549	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
43	CTCF	chr1:213418020-213418170	GM12870	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
44	CTCF	chr1:213418040-213418190	HMEC	breast:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
45	CTCF	chr1:213418100-213418250	AG04450	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
46	CTCF	chr1:213418080-213418230	GM12870	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
47	CTCF	chr1:213418040-213418190	HEK293	kidney:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
48	CTCF	chr1:213418040-213418190	GM12869	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
49	CTCF	chr1:213418040-213418190	AG04450	lung:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128
50	CTCF	chr1:213418040-213418190	GM12875	blood:	n/a	chr1:213418113-213418121 chr1:213418111-213418127 chr1:213418113-213418126 chr1:213418112-213418133 chr1:213418110-213418128

No.	Distal block	Cell Line	Cell type
1	chr1:213418757..213420521-chr1:213420795..213423532,2	K562	blood:
2	chr1:213408487..213410031-chr1:213414324..213416329,2	K562	blood:
3	chr1:213405078..213407428-chr1:213458002..213459532,2	K562	blood:
4	chr1:213410280..213412046-chr1:213412206..213414016,2	K562	blood:
5	chr1:213411859..213414692-chr1:214502325..214505233,2	MCF-7	breast:
6	chr1:213404542..213407236-chr1:213407336..213409957,4	K562	blood:
7	chr1:213412075..213413752-chr1:213416133..213417762,2	K562	blood:
8	chr1:213412075..213413752-chr1:213416133..213417762,2	K562	blood:
9	chr1:213404542..213407236-chr1:213407336..213409957,4	K562	blood:
10	chr1:213402752..213406485-chr1:213407336..213409519,4	K562	blood:
11	chr1:213403677..213405809-chr1:213417611..213420173,2	K562	blood:
12	chr1:213418757..213420521-chr1:213420795..213423532,2	K562	blood:
13	chr1:213420850..213423697-chr1:213427535..213429771,2	K562	blood:
14	chr1:213410280..213412046-chr1:213412206..213414016,2	K562	blood:
15	chr1:213402752..213406485-chr1:213407336..213409519,4	K562	blood:

Variant related genes	Relation type
RPS6KC1	TF binding region
ENSG00000136643	chromatin interactions
ENSG00000143499	chromatin interactions

Extended variants
information (count: 524 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:524 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531775938	chr1:213406259-213406260	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs184844985	chr1:213406312-213406313	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs562246406	chr1:213406313-213406314	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529350766	chr1:213406345-213406346	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs76749076	chr1:213406359-213406360	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138863631	chr1:213406381-213406382	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs12075302	chr1:213406395-213406396	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs75645450	chr1:213406401-213406402	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs553859915	chr1:213406404-213406405	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569849793	chr1:213406409-213406410	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs573650760	chr1:213406419-213406420	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188638760	chr1:213406478-213406479	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543245867	chr1:213406532-213406533	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs555040939	chr1:213406591-213406592	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192758043	chr1:213406596-213406597	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs78848142	chr1:213406619-213406620	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs554413804	chr1:213406727-213406728	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs572623351	chr1:213406786-213406787	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs546415081	chr1:213406787-213406788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs576661684	chr1:213406867-213406868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs17020291	chr1:213406883-213406884	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs371733327	chr1:213406910-213406911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545736209	chr1:213406934-213406935	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184100071	chr1:213406949-213406950	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs77150991	chr1:213406960-213406961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543828804	chr1:213406965-213406966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189869703	chr1:213406966-213406967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs376037211	chr1:213406993-213406994	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144158356	chr1:213407087-213407088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79238502	chr1:213407129-213407130	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541085772	chr1:213407137-213407138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148698338	chr1:213407156-213407157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141257560	chr1:213407162-213407163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551278210	chr1:213407239-213407240	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181157629	chr1:213407274-213407275	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532037911	chr1:213407283-213407284	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs370105845	chr1:213407318-213407319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572972769	chr1:213407358-213407359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs114148040	chr1:213407359-213407360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs61832469	chr1:213407375-213407376	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs527719146	chr1:213407380-213407381	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs34919075	chr1:213407411-213407412	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs541066570	chr1:213407419-213407420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373634151	chr1:213407430-213407431	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147415783	chr1:213407434-213407435	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs72745847	chr1:213407542-213407543	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs139519708	chr1:213407591-213407592	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs184492099	chr1:213407612-213407613	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs188861336	chr1:213407773-213407774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77453211	chr1:213407809-213407810	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Medulloblastoma	16783165	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Holoprosencephaly	19184110	CNVD
Breast cancer	21069454	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Mental retardation	19951919	CNVD
Non-syndromic sensorineural hearing loss	17873649	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:346 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:213326600-213422200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr1:213340600-213424600	Weak transcription	Pancreas	Pancrea
3	chr1:213362200-213415400	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr1:213370800-213427600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr1:213372600-213413800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr1:213372800-213414000	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr1:213373000-213414200	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:213373000-213423000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
9	chr1:213373200-213417000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr1:213376800-213414200	Weak transcription	Brain Anterior Caudate	brain
11	chr1:213378800-213421200	Weak transcription	Fetal Kidney	kidney
12	chr1:213381600-213425000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr1:213385600-213407000	Weak transcription	Stomach Mucosa	stomach
14	chr1:213387400-213414000	Weak transcription	Duodenum Smooth Muscle	Duodenum
15	chr1:213388000-213414400	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr1:213388000-213424600	Weak transcription	Gastric	stomach
17	chr1:213388200-213414000	Weak transcription	Aorta	Aorta
18	chr1:213388200-213414000	Weak transcription	Liver	Liver
19	chr1:213388200-213414200	Weak transcription	Ovary	ovary
20	chr1:213388200-213417200	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr1:213388200-213426200	Weak transcription	Lung	lung
22	chr1:213388200-213455400	Weak transcription	Placenta	Placenta
23	chr1:213388400-213407400	Weak transcription	Fetal Stomach	stomach
24	chr1:213388400-213407600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr1:213388400-213414000	Weak transcription	Fetal Muscle Leg	muscle
26	chr1:213388400-213414200	Weak transcription	Primary hematopoietic stem cells	blood
27	chr1:213388400-213414200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr1:213388400-213414200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
29	chr1:213388600-213418200	Weak transcription	Fetal Intestine Small	intestine
30	chr1:213391200-213439200	Weak transcription	Primary B cells from cord blood	blood
31	chr1:213394400-213420200	Weak transcription	GM12878-XiMat	blood
32	chr1:213398600-213427200	Weak transcription	Colon Smooth Muscle	Colon
33	chr1:213399600-213418000	Weak transcription	Primary neutrophils fromperipheralblood	blood
34	chr1:213401200-213447400	Weak transcription	Small Intestine	intestine
35	chr1:213402800-213454800	Weak transcription	Brain Substantia Nigra	brain
36	chr1:213403000-213414400	Weak transcription	Brain Cingulate Gyrus	brain
37	chr1:213403200-213407400	Weak transcription	Fetal Intestine Large	intestine
38	chr1:213403200-213418000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr1:213403400-213414000	Weak transcription	Dnd41	blood
40	chr1:213403400-213414800	Weak transcription	Brain Germinal Matrix	brain
41	chr1:213403600-213408200	Weak transcription	HepG2	liver
42	chr1:213403800-213412200	Weak transcription	Esophagus	oesophagus
43	chr1:213404000-213414000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr1:213404200-213416400	Weak transcription	Fetal Thymus	thymus
45	chr1:213404400-213412200	Strong transcription	Monocytes-CD14+_RO01746	blood
46	chr1:213404600-213409000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr1:213404800-213414200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr1:213405000-213406800	Strong transcription	Primary T cells fromperipheralblood	blood
49	chr1:213405000-213408600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
50	chr1:213405200-213406800	Enhancers	HUES64 Cell Line	embryonic stem cell

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