Variant report

Variant	nsv997360
Chromosome Location	chr1:169892284-169946436
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	chr1:169898085-169898379	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:169898074-169898510	K562	blood:	n/a	n/a
3	BCLAF1	chr1:169897998-169898407	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:169895312-169895694	GM12878	blood:	n/a	n/a
5	CBX3	chr1:169897990-169898402	HCT-116	colon:	n/a	n/a
6	CEBPB	chr1:169915475-169915783	IMR90	lung:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
7	CEBPB	chr1:169895158-169895662	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:169897984-169898391	HCT-116	colon:	n/a	n/a
9	CEBPB	chr1:169920105-169920380	A549	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
10	CEBPB	chr1:169915401-169915893	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
11	CEBPB	chr1:169920089-169920421	IMR90	lung:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
12	CEBPB	chr1:169915309-169915804	MCF-7	breast:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
13	CEBPB	chr1:169920135-169920408	HepG2	liver:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
14	CEBPB	chr1:169920115-169920364	K562	blood:	n/a	chr1:169920249-169920258 chr1:169920248-169920259 chr1:169920247-169920258
15	CEBPB	chr1:169915356-169915820	Hela-S3	cervix:	n/a	chr1:169915539-169915552 chr1:169915541-169915550
16	CHD1	chr1:169898365-169898449	GM12878	blood:	n/a	n/a
17	CTCF	chr1:169897840-169897990	NHLF	lung:	n/a	n/a
18	CTCF	chr1:169898135-169898343	MCF-7	breast:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
19	CTCF	chr1:169898140-169898290	HepG2	liver:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
20	CTCF	chr1:169898160-169898310	AG04450	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
21	CTCF	chr1:169898180-169898330	HRPEpiC	eye:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
22	CTCF	chr1:169898079-169898332	SK-N-SH_RA	brain:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
23	CTCF	chr1:169898139-169898327	LNCaP	prostate:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
24	CTCF	chr1:169897990-169898459	MCF-7	breast:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
25	CTCF	chr1:169898300-169898450	A549	lung:	n/a	n/a
26	CTCF	chr1:169898120-169898270	MCF-7	breast:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
27	CTCF	chr1:169898140-169898290	GM12801	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
28	CTCF	chr1:169898140-169898290	HUVEC	blood vessel:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
29	CTCF	chr1:169898151-169898327	GM10248	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
30	CTCF	chr1:169897868-169898622	A549	lung:	n/a	chr1:169898236-169898244 chr1:169898233-169898254 chr1:169898231-169898249
31	CTCF	chr1:169898160-169898310	Caco-2	colon:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
32	CTCF	chr1:169898100-169898250	A549	lung:	n/a	chr1:169898236-169898244 chr1:169898231-169898249
33	CTCF	chr1:169898112-169898370	Pancreas_OC	pancreas:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
34	CTCF	chr1:169898180-169898330	GM12870	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
35	CTCF	chr1:169898180-169898330	HA-sp	spinal cord:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
36	CTCF	chr1:169898121-169898364	Lung_OC	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
37	CTCF	chr1:169914572-169914617	MCF-7	breast:	n/a	n/a
38	CTCF	chr1:169898007-169898371	H1-hESC	embryonic stem cell:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
39	CTCF	chr1:169898080-169898230	MCF-7	breast:	n/a	n/a
40	CTCF	chr1:169898100-169898250	GM12866	blood:	n/a	chr1:169898236-169898244 chr1:169898231-169898249
41	CTCF	chr1:169898143-169898326	GM10266	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
42	CTCF	chr1:169898160-169898310	HEEpiC	esophagus:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
43	CTCF	chr1:169898180-169898330	HEEpiC	esophagus:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
44	CTCF	chr1:169898160-169898310	HBMEC	blood vessel:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
45	CTCF	chr1:169898160-169898310	GM12872	blood:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
46	CTCF	chr1:169898106-169898306	SK-N-SH_RA	brain:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
47	CTCF	chr1:169898031-169898455	IMR90	lung:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
48	CTCF	chr1:169898180-169898330	BJ	skin:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
49	CTCF	chr1:169897879-169898620	SK-N-SH	brain:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249
50	CTCF	chr1:169898100-169898358	Hela-S3	cervix:	n/a	chr1:169898233-169898254 chr1:169898236-169898244 chr1:169898231-169898249

No.	Distal block	Cell Line	Cell type
1	chr1:169883530..169886106-chr1:169901752..169904376,3	K562	blood:
2	chr1:169863023..169865011-chr1:169913232..169916470,3	MCF-7	breast:
3	chr1:169927495..169930307-chr1:170507858..170509808,2	K562	blood:
4	chr1:169861783..169864814-chr1:169892837..169895451,3	MCF-7	breast:
5	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
6	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
7	chr1:169885836..169887922-chr1:169893783..169895856,2	MCF-7	breast:
8	chr1:169894940..169897093-chr1:169912669..169915603,2	MCF-7	breast:
9	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
10	chr1:169819515..169822344-chr1:169896401..169898488,2	MCF-7	breast:
11	chr1:169906887..169908799-chr1:169914040..169915551,2	MCF-7	breast:
12	chr1:169897805..169898496-chr1:170898617..170899529,4	MCF-7	breast:
13	chr1:169858457..169860973-chr1:169907396..169909921,2	MCF-7	breast:
14	chr1:169909334..169912008-chr1:170041825..170044429,2	MCF-7	breast:
15	chr1:169891530..169894353-chr1:169899147..169901987,3	K562	blood:
16	chr1:169898316..169900651-chr1:169903000..169904751,2	K562	blood:
17	chr1:169904469..169905208-chr1:169979740..169980542,2	MCF-7	breast:
18	chr1:169887846..169894353-chr1:169898169..169903456,7	K562	blood:
19	chr1:169862245..169864105-chr1:169894595..169896381,2	MCF-7	breast:
20	chr1:169862018..169863594-chr1:169891120..169892804,2	MCF-7	breast:
21	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
22	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
23	chr1:169896264..169898992-chr1:170499654..170502527,2	MCF-7	breast:
24	chr1:169897891..169898773-chr1:170898615..170899541,2	MCF-7	breast:
25	chr1:169897753..169898707-chr1:170850760..170851657,6	MCF-7	breast:
26	chr1:169909516..169911412-chr20:55839152..55841163,2	MCF-7	breast:
27	chr1:169860365..169863802-chr1:169902105..169905662,4	MCF-7	breast:
28	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
29	chr1:169897755..169898590-chr1:170734743..170735498,2	MCF-7	breast:
30	chr1:169903817..169906654-chr1:169908531..169910584,2	K562	blood:
31	chr1:169942236..169943172-chrX:26753938..26754794,2	MCF-7	breast:
32	chr1:169907968..169909649-chr1:169910615..169913475,2	K562	blood:
33	chr1:169891530..169894353-chr1:169899147..169901987,3	K562	blood:
34	chr1:169887846..169894353-chr1:169898169..169903456,7	K562	blood:
35	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:
36	chr1:169861655..169864221-chr1:169940931..169943553,2	MCF-7	breast:
37	chr1:169913226..169915577-chr1:169917390..169920061,2	MCF-7	breast:
38	chr1:169915601..169917304-chr1:169919424..169921809,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SCYL3-1	chr1:169927085-169927387	NONHSAT007483

Variant related genes	Relation type
RN7SL269P	TF binding region
ENSG00000075945	chromatin interactions
ENSG00000000457	chromatin interactions
ENSG00000231407	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000120370	chromatin interactions

Extended variants
information (count: 1806 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1806 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575147	chr1:169892284-169892285	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565520442	chr1:169892292-169892293	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs80175861	chr1:169892318-169892319	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs183688168	chr1:169892335-169892336	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs559613641	chr1:169892356-169892357	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs188007182	chr1:169892390-169892391	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs34536097	chr1:169892423-169892424	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs548188507	chr1:169892451-169892452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555566724	chr1:169892504-169892505	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs574823024	chr1:169892517-169892518	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs569670695	chr1:169892572-169892573	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs143537290	chr1:169892644-169892645	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs150872832	chr1:169892648-169892649	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs386636670	chr1:169892651-169892652	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549801038	chr1:169892654-169892655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs590181	chr1:169892661-169892662	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs538430174	chr1:169892711-169892712	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs553902283	chr1:169892720-169892721	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs374444979	chr1:169892761-169892762	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150988451	chr1:169892769-169892770	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs536311189	chr1:169892770-169892771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs374010975	chr1:169892872-169892873	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539941499	chr1:169892891-169892892	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs554606370	chr1:169892932-169892933	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs74387271	chr1:169892936-169892937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs35342344	chr1:169892954-169892955	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs544167981	chr1:169892962-169892963	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs558965278	chr1:169892966-169892967	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs16862753	chr1:169892970-169892971	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs544920368	chr1:169892973-169892974	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs144653374	chr1:169893027-169893028	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs77584355	chr1:169893132-169893133	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs397735676	chr1:169893140-169893141	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs372244142	chr1:169893148-169893149	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs138626626	chr1:169893149-169893150	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs181411199	chr1:169893154-169893155	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs186172715	chr1:169893155-169893156	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs603246	chr1:169893204-169893205	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs550074543	chr1:169893245-169893246	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs377075758	chr1:169893262-169893263	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs544008	chr1:169893330-169893331	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs141521515	chr1:169893350-169893351	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs547282433	chr1:169893486-169893487	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565832221	chr1:169893503-169893504	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs563112935	chr1:169893504-169893505	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs57813710	chr1:169893523-169893524	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs191421239	chr1:169893555-169893556	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs368591016	chr1:169893569-169893570	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs536668729	chr1:169893603-169893604	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs145253298	chr1:169893613-169893614	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Glioblastoma multiforme	21080181	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
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
Breast cancer	21509527	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
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169876200-169903600	Weak transcription	Aorta	Aorta
2	chr1:169878400-169895200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr1:169878400-169946200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr1:169878600-169895000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr1:169880200-169892800	Weak transcription	Fetal Heart	heart
6	chr1:169881400-169901000	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr1:169884200-169913000	Weak transcription	Rectal Mucosa Donor 29	rectum
8	chr1:169884600-169892800	Weak transcription	Pancreas	Pancrea
9	chr1:169884600-169895200	Weak transcription	Fetal Intestine Small	intestine
10	chr1:169884600-169900600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr1:169884600-169900600	Weak transcription	NHDF-Ad	bronchial
12	chr1:169885200-169900800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr1:169885400-169894000	Weak transcription	Right Ventricle	heart
14	chr1:169885400-169913200	Weak transcription	Ovary	ovary
15	chr1:169885600-169903200	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr1:169885800-169896600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
17	chr1:169885800-169898000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr1:169886000-169894000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:169886400-169894600	Weak transcription	Primary B cells from cord blood	blood
20	chr1:169886400-169895200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:169886400-169913000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr1:169886600-169915600	Weak transcription	Stomach Smooth Muscle	stomach
23	chr1:169887000-169911400	Weak transcription	Left Ventricle	heart
24	chr1:169888400-169892400	Weak transcription	Fetal Brain Male	brain
25	chr1:169888800-169894800	Weak transcription	GM12878-XiMat	blood
26	chr1:169888800-169900600	Weak transcription	Fetal Stomach	stomach
27	chr1:169889000-169895200	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr1:169889600-169900600	Weak transcription	Fetal Lung	lung
29	chr1:169889800-169898000	Weak transcription	Brain Inferior Temporal Lobe	brain
30	chr1:169890200-169895200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr1:169890800-169893600	Weak transcription	Psoas Muscle	Psoas
32	chr1:169890800-169894800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr1:169890800-169906200	Weak transcription	Primary T helper cells PMA-I stimulated	--
34	chr1:169891000-169895200	Weak transcription	Primary T cells from cord blood	blood
35	chr1:169891000-169896800	Weak transcription	Primary T helper cells fromperipheralblood	blood
36	chr1:169891000-169898200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr1:169891000-169911400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr1:169891000-169913200	Weak transcription	Adipose Nuclei	Adipose
39	chr1:169891200-169894800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr1:169891800-169894200	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
41	chr1:169892800-169893000	Enhancers	Pancreas	Pancrea
42	chr1:169892800-169895600	Enhancers	Fetal Heart	heart
43	chr1:169894000-169894200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr1:169894000-169894200	Enhancers	Right Ventricle	heart
45	chr1:169894000-169895400	Enhancers	HSMMtube	muscle
46	chr1:169894200-169894400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr1:169894200-169894400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:169894200-169903400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr1:169894600-169894800	Weak transcription	Dnd41	blood
50	chr1:169894600-169895400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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