Variant report

Variant	nsv872554
Chromosome Location	chr1:174209978-174291950
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	chr1:174235526-174236877	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:174243609-174243996	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:174231891-174232149	K562	blood:	n/a	n/a
4	ARID3A	chr1:174227162-174227507	K562	blood:	n/a	n/a
5	ARID3A	chr1:174227171-174227530	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:174239214-174239484	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:174231871-174232199	HepG2	liver:	n/a	n/a
8	ATF1	chr1:174277912-174277913	K562	blood:	n/a	n/a
9	ATF1	chr1:174235618-174235768	K562	blood:	n/a	n/a
10	ATF1	chr1:174263197-174263318	K562	blood:	n/a	n/a
11	ATF2	chr1:174245148-174245601	GM12878	blood:	n/a	n/a
12	BACH1	chr1:174270567-174271092	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCLAF1	chr1:174245097-174245620	GM12878	blood:	n/a	n/a
14	CBX3	chr1:174290094-174290435	K562	blood:	n/a	n/a
15	CBX3	chr1:174284427-174284759	K562	blood:	n/a	n/a
16	CBX3	chr1:174270523-174270977	K562	blood:	n/a	n/a
17	CBX3	chr1:174284403-174284874	K562	blood:	n/a	n/a
18	CBX3	chr1:174289992-174290425	K562	blood:	n/a	n/a
19	CCNT2	chr1:174226984-174227184	K562	blood:	n/a	n/a
20	CEBPB	chr1:174249004-174249104	K562	blood:	n/a	n/a
21	CEBPB	chr1:174248885-174249202	IMR90	lung:	n/a	n/a
22	CEBPB	chr1:174265481-174265826	Hela-S3	cervix:	n/a	chr1:174265652-174265661 chr1:174265652-174265661 chr1:174265650-174265661 chr1:174265652-174265661
23	CEBPB	chr1:174265481-174265835	HepG2	liver:	n/a	chr1:174265652-174265661 chr1:174265652-174265661 chr1:174265650-174265661 chr1:174265652-174265661
24	CEBPB	chr1:174265469-174265836	IMR90	lung:	n/a	chr1:174265652-174265661 chr1:174265652-174265661 chr1:174265650-174265661 chr1:174265652-174265661
25	CEBPB	chr1:174236179-174236683	HepG2	liver:	n/a	chr1:174236334-174236345
26	CEBPB	chr1:174253072-174253325	A549	lung:	n/a	chr1:174253181-174253192
27	CEBPB	chr1:174235492-174235906	HepG2	liver:	n/a	chr1:174235715-174235726
28	CEBPB	chr1:174270541-174270847	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr1:174265468-174265834	K562	blood:	n/a	chr1:174265652-174265661 chr1:174265652-174265661 chr1:174265650-174265661 chr1:174265652-174265661
30	CEBPB	chr1:174265507-174265829	H1-hESC	embryonic stem cell:	n/a	chr1:174265652-174265661 chr1:174265652-174265661 chr1:174265650-174265661 chr1:174265652-174265661
31	CEBPB	chr1:174236227-174236507	K562	blood:	n/a	chr1:174236334-174236345
32	CEBPB	chr1:174243605-174243895	HepG2	liver:	n/a	chr1:174243725-174243736
33	CEBPB	chr1:174271180-174271236	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr1:174265485-174265814	A549	lung:	n/a	chr1:174265652-174265661 chr1:174265652-174265661 chr1:174265650-174265661 chr1:174265652-174265661
35	CEBPB	chr1:174265508-174265786	K562	blood:	n/a	chr1:174265652-174265661 chr1:174265652-174265661 chr1:174265650-174265661 chr1:174265652-174265661
36	CEBPB	chr1:174291213-174291328	HepG2	liver:	n/a	n/a
37	CEBPB	chr1:174277885-174278089	K562	blood:	n/a	n/a
38	CEBPB	chr1:174253075-174253259	HepG2	liver:	n/a	chr1:174253181-174253192
39	CEBPB	chr1:174277440-174277448	A549	lung:	n/a	n/a
40	CEBPB	chr1:174277912-174277999	A549	lung:	n/a	n/a
41	CEBPB	chr1:174277430-174277450	K562	blood:	n/a	n/a
42	CEBPB	chr1:174277808-174278120	K562	blood:	n/a	n/a
43	CEBPB	chr1:174243592-174243914	IMR90	lung:	n/a	chr1:174243725-174243736
44	CEBPB	chr1:174277825-174278104	K562	blood:	n/a	n/a
45	CTCF	chr1:174227320-174227470	HFF	foreskin:	n/a	chr1:174227383-174227401 chr1:174227386-174227394 chr1:174227386-174227399 chr1:174227385-174227406
46	CTCF	chr1:174227300-174227450	GM12878	blood:	n/a	chr1:174227383-174227401 chr1:174227386-174227394 chr1:174227386-174227399 chr1:174227385-174227406
47	CTCF	chr1:174231760-174231910	HAc	cerebellar:	n/a	n/a
48	CTCF	chr1:174231940-174232090	GM12873	blood:	n/a	n/a
49	CTCF	chr1:174227300-174227450	GM12874	blood:	n/a	chr1:174227383-174227401 chr1:174227386-174227394 chr1:174227386-174227399 chr1:174227385-174227406
50	CTCF	chr1:174231791-174232240	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:174269404..174272933-chr1:174275940..174280582,4	MCF-7	breast:
2	chr1:174225306..174226872-chr1:174233081..174234854,2	K562	blood:
3	chr1:174209547..174211969-chr1:174214945..174217167,2	MCF-7	breast:
4	chr1:174223640..174225967-chr1:174230477..174232706,2	K562	blood:
5	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
6	chr1:174225894..174227606-chr1:174968644..174970574,2	MCF-7	breast:
7	chr1:174226668..174227633-chr1:174712845..174713766,3	MCF-7	breast:
8	chr1:174217947..174220664-chr1:174222845..174224894,3	K562	blood:
9	chr1:174215485..174217028-chr1:174218870..174220698,2	MCF-7	breast:
10	chr1:174215485..174217028-chr1:174218870..174220698,2	MCF-7	breast:
11	chr1:174226894..174227818-chr1:174695415..174695933,2	MCF-7	breast:
12	chr1:173834767..173837428-chr1:174208360..174210582,3	MCF-7	breast:
13	chr1:174236338..174237956-chr1:174241519..174243229,2	K562	blood:
14	chr1:174209681..174211217-chr1:174211648..174214510,2	K562	blood:
15	chr1:174257821..174260787-chr1:174268762..174270773,2	MCF-7	breast:
16	chr1:173923747..173925915-chr1:174209553..174212014,2	MCF-7	breast:
17	chr1:174208904..174211373-chr1:174212924..174214774,3	MCF-7	breast:
18	chr1:174214049..174216342-chr7:121419636..121421271,2	MCF-7	breast:
19	chr1:173989061..173991259-chr1:174208907..174211636,3	MCF-7	breast:
20	chr1:174190274..174193024-chr1:174230012..174232463,2	K562	blood:
21	chr1:174207103..174211366-chr1:174211395..174216784,8	MCF-7	breast:
22	chr1:174226899..174227872-chr1:174716763..174717382,2	MCF-7	breast:
23	chr1:174236001..174238178-chr1:174240503..174243812,3	K562	blood:
24	chr1:174209547..174211969-chr1:174214945..174217167,2	MCF-7	breast:
25	chr1:174238690..174241615-chr1:174967478..174969557,2	MCF-7	breast:
26	chr1:174217947..174220664-chr1:174222845..174224894,3	K562	blood:
27	chr1:174269404..174272933-chr1:174275940..174280582,4	MCF-7	breast:
28	chr1:174208904..174211373-chr1:174212924..174214774,3	MCF-7	breast:
29	chr1:174257821..174260787-chr1:174268762..174270773,2	MCF-7	breast:
30	chr1:174225306..174226872-chr1:174233081..174234854,2	K562	blood:
31	chr1:174227366..174227954-chr1:174695618..174696250,2	K562	blood:
32	chr1:174062652..174063623-chr1:174227311..174228008,2	MCF-7	breast:
33	chr1:174246288..174247946-chr1:174254999..174256826,2	K562	blood:
34	chr1:174231956..174232498-chr1:174695300..174696266,2	MCF-7	breast:
35	chr1:174236001..174238178-chr1:174240503..174243812,3	K562	blood:
36	chr1:174246288..174247946-chr1:174254999..174256826,2	K562	blood:
37	chr1:174223640..174225967-chr1:174230477..174232706,2	K562	blood:
38	chr1:174208598..174210493-chr1:174218021..174220094,2	MCF-7	breast:
39	chr1:174287001..174289924-chr1:174290747..174293393,2	K562	blood:
40	chr1:174231569..174233206-chr1:174712799..174714098,7	K562	blood:
41	chr1:174231547..174232813-chr1:174695220..174696649,6	MCF-7	breast:
42	chr1:174209681..174211217-chr1:174211648..174214510,2	K562	blood:
43	chr1:174207103..174211366-chr1:174211395..174216784,8	MCF-7	breast:
44	chr1:174227280..174227817-chr1:174712805..174713329,2	K562	blood:
45	chr1:174208598..174210493-chr1:174218021..174220094,2	MCF-7	breast:
46	chr1:174236338..174237956-chr1:174241519..174243229,2	K562	blood:

Variant related genes	Relation type
RABGAP1L	TF binding region
ENSG00000208317	chromatin interactions
ENSG00000116161	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000234741	chromatin interactions

Extended variants
information (count: 2785 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2785 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7535987	chr1:174209978-174209979	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs570826840	chr1:174210060-174210061	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs200986126	chr1:174210076-174210077	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs71958106	chr1:174210077-174210078	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs543933413	chr1:174210197-174210198	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs562085243	chr1:174210229-174210230	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs550281556	chr1:174210260-174210261	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs150948492	chr1:174210273-174210274	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs577808972	chr1:174210274-174210275	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs540018930	chr1:174210319-174210320	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs560050400	chr1:174210398-174210399	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs182660613	chr1:174210427-174210428	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs548968645	chr1:174210440-174210441	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs143230337	chr1:174210457-174210458	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs562501298	chr1:174210476-174210477	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs531721010	chr1:174210486-174210487	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs551629467	chr1:174210539-174210540	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs61628461	chr1:174210540-174210541	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs534160723	chr1:174210556-174210557	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs192248297	chr1:174210578-174210579	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs375717257	chr1:174210581-174210582	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs375550164	chr1:174210617-174210618	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs368672299	chr1:174210631-174210632	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200126832	chr1:174210633-174210634	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs142743501	chr1:174210642-174210643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143661013	chr1:174210668-174210669	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140628487	chr1:174210684-174210685	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575173120	chr1:174210689-174210690	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537847739	chr1:174210704-174210705	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138264771	chr1:174210707-174210708	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs557596672	chr1:174210714-174210715	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376064634	chr1:174210741-174210742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144504710	chr1:174210750-174210751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs371333673	chr1:174210790-174210791	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373653316	chr1:174210791-174210792	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs12136358	chr1:174210910-174210911	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs528461479	chr1:174210977-174210978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148425348	chr1:174211007-174211008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs375590875	chr1:174211018-174211019	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs562797348	chr1:174211047-174211048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531636072	chr1:174211085-174211086	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545369136	chr1:174211097-174211098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs73036620	chr1:174211117-174211118	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182665814	chr1:174211156-174211157	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548016259	chr1:174211162-174211163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142526108	chr1:174211221-174211222	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146423043	chr1:174211277-174211278	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs532398547	chr1:174211381-174211382	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570309031	chr1:174211481-174211482	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187666815	chr1:174211504-174211505	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	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
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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	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
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	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
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1264 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:174176000-174222400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:174176800-174222400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr1:174177200-174212000	Weak transcription	Lung	lung
4	chr1:174178600-174212200	Weak transcription	Psoas Muscle	Psoas
5	chr1:174186600-174216600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:174186800-174212800	Weak transcription	Fetal Heart	heart
7	chr1:174186800-174213200	Weak transcription	Ovary	ovary
8	chr1:174186800-174217000	Weak transcription	Brain Angular Gyrus	brain
9	chr1:174186800-174232000	Weak transcription	HSMMtube	muscle
10	chr1:174187000-174217000	Weak transcription	Pancreas	Pancrea
11	chr1:174188600-174213400	Weak transcription	Spleen	Spleen
12	chr1:174189000-174232000	Weak transcription	HSMM	muscle
13	chr1:174189200-174216800	Weak transcription	Small Intestine	intestine
14	chr1:174189600-174215400	Weak transcription	NH-A	brain
15	chr1:174191000-174215600	Weak transcription	Fetal Brain Male	brain
16	chr1:174191400-174215400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr1:174191400-174232000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr1:174191600-174213400	Weak transcription	Thymus	Thymus
19	chr1:174191600-174232200	Weak transcription	Brain Substantia Nigra	brain
20	chr1:174191800-174215600	Weak transcription	Brain Anterior Caudate	brain
21	chr1:174192000-174215200	Weak transcription	HMEC	breast
22	chr1:174192000-174219400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr1:174192200-174213200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr1:174192400-174224600	Weak transcription	Fetal Thymus	thymus
25	chr1:174192600-174213600	Weak transcription	Fetal Intestine Small	intestine
26	chr1:174193200-174212800	Weak transcription	Hela-S3	cervix
27	chr1:174197000-174213400	Weak transcription	Colonic Mucosa	Colon
28	chr1:174198800-174213400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr1:174199400-174213400	Weak transcription	Gastric	stomach
30	chr1:174200600-174216000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
31	chr1:174200800-174213600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr1:174200800-174249200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
33	chr1:174201000-174213200	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:174201000-174213400	Weak transcription	Aorta	Aorta
35	chr1:174201000-174217600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr1:174201000-174221800	Weak transcription	Fetal Muscle Trunk	muscle
37	chr1:174201000-174249800	Weak transcription	Primary hematopoietic stem cells	blood
38	chr1:174201200-174212200	Weak transcription	Primary neutrophils fromperipheralblood	blood
39	chr1:174201200-174213400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr1:174201200-174218200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr1:174201200-174221400	Weak transcription	NHDF-Ad	bronchial
42	chr1:174201400-174213400	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr1:174201400-174213400	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:174201600-174210800	Weak transcription	Duodenum Mucosa	Duodenum
45	chr1:174201800-174213400	Weak transcription	Fetal Stomach	stomach
46	chr1:174202200-174210600	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr1:174202200-174210600	Weak transcription	Monocytes-CD14+_RO01746	blood
48	chr1:174202200-174212000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr1:174202200-174213400	Weak transcription	Fetal Muscle Leg	muscle
50	chr1:174202400-174210000	Weak transcription	Primary T cells from cord blood	blood

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