Variant report

Variant	nsv825197
Chromosome Location	chr9:140723503-140759174
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	BATF	chr9:140731105-140731321	GM12878	blood:	n/a	n/a
2	BATF	chr9:140747930-140748125	GM12878	blood:	n/a	n/a
3	BHLHE40	chr9:140731130-140731329	K562	blood:	n/a	n/a
4	CCNT2	chr9:140729504-140729518	K562	blood:	n/a	n/a
5	CEBPB	chr9:140731082-140731475	H1-hESC	embryonic stem cell:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
6	CEBPB	chr9:140731058-140731398	HepG2	liver:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
7	CEBPB	chr9:140746440-140746708	K562	blood:	n/a	n/a
8	CEBPB	chr9:140733435-140733635	A549	lung:	n/a	chr9:140733512-140733523 chr9:140733514-140733523 chr9:140733513-140733524
9	CEBPB	chr9:140731077-140731543	K562	blood:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
10	CEBPB	chr9:140731160-140731312	HepG2	liver:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
11	CEBPB	chr9:140746423-140746547	A549	lung:	n/a	n/a
12	CEBPB	chr9:140731077-140731484	Hela-S3	cervix:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
13	CEBPB	chr9:140731027-140731466	K562	blood:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
14	CEBPB	chr9:140731134-140731426	ECC-1	luminal epithelium:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
15	CEBPB	chr9:140733385-140733586	K562	blood:	n/a	chr9:140733512-140733523 chr9:140733514-140733523 chr9:140733513-140733524
16	CEBPB	chr9:140733435-140733667	HepG2	liver:	n/a	chr9:140733512-140733523 chr9:140733514-140733523 chr9:140733513-140733524
17	CEBPB	chr9:140730983-140731575	MCF-7	breast:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
18	CEBPB	chr9:140731101-140731454	HepG2	liver:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
19	CEBPB	chr9:140746402-140746765	MCF-7	breast:	n/a	n/a
20	CEBPB	chr9:140731088-140731472	A549	lung:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
21	CEBPB	chr9:140746103-140746326	HepG2	liver:	n/a	n/a
22	CEBPB	chr9:140731082-140731461	IMR90	lung:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
23	CEBPB	chr9:140731077-140731523	A549	lung:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
24	CEBPB	chr9:140733389-140733674	IMR90	lung:	n/a	chr9:140733512-140733523 chr9:140733514-140733523 chr9:140733513-140733524
25	CEBPB	chr9:140745962-140746844	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr9:140731014-140731604	MCF-7	breast:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
27	CEBPB	chr9:140746182-140746218	A549	lung:	n/a	n/a
28	CEBPB	chr9:140731067-140731469	HepG2	liver:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
29	CEBPB	chr9:140730916-140731619	A549	lung:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
30	CEBPB	chr9:140731131-140731378	K562	blood:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
31	CEBPB	chr9:140731069-140731514	ECC-1	luminal epithelium:	n/a	chr9:140731272-140731281 chr9:140731270-140731283 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731272-140731281 chr9:140731270-140731281
32	CTCF	chr9:140731440-140731590	HepG2	liver:	n/a	n/a
33	CTCF	chr9:140751376-140751502	MCF-7	breast:	n/a	n/a
34	CTCF	chr9:140751420-140751570	HepG2	liver:	n/a	n/a
35	CTCF	chr9:140731428-140731695	GM12878	blood:	n/a	n/a
36	CTCF	chr9:140731480-140731630	A549	lung:	n/a	n/a
37	CTCF	chr9:140731420-140731570	HEK293	kidney:	n/a	n/a
38	CTCF	chr9:140751324-140751510	HepG2	liver:	n/a	n/a
39	CTCF	chr9:140730764-140730770	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr9:140731520-140731670	GM12873	blood:	n/a	n/a
41	CTCF	chr9:140731532-140731592	GM10266	blood:	n/a	n/a
42	CTCF	chr9:140731498-140731630	Hela-S3	cervix:	n/a	n/a
43	CTCF	chr9:140731484-140731650	MCF-7	breast:	n/a	n/a
44	CTCF	chr9:140731442-140731679	MCF-7	breast:	n/a	n/a
45	CTCF	chr9:140735499-140735608	GM19239	blood:	n/a	n/a
46	CTCF	chr9:140731520-140731670	K562	blood:	n/a	n/a
47	CTCF	chr9:140731440-140731590	GM12864	blood:	n/a	n/a
48	CTCF	chr9:140731500-140731650	GM12872	blood:	n/a	n/a
49	CTCF	chr9:140731500-140731650	HCT-116	colon:	n/a	n/a
50	CTCF	chr9:140751370-140751521	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140727297-140727347	AoSMC	blood vessel:	n/a
2	chr9:140728491-140728541	SK-N-SH_RA	brain:	n/a
3	chr9:140735359-140735409	Hela-S3	cervix:	n/a
4	chr9:140727297-140727347	AoSMC	blood vessel:	n/a
5	chr9:140728491-140728541	SK-N-SH_RA	brain:	n/a
6	chr9:140735359-140735409	Hela-S3	cervix:	n/a
7	chr9:140738145-140738195	A549	lung:	n/a
8	chr9:140733714-140733764	GM12891	blood:	n/a
9	chr9:140729712-140729762	U87	brain:	n/a
10	chr9:140730806-140730856	AoSMC	blood vessel:	n/a
11	chr9:140731022-140731072	NH-A	brain:	n/a
12	chr9:140729241-140729291	H1-hESC	embryonic stem cell:	embryo
13	chr9:140726863-140726913	SKMC	muscle:	n/a
14	chr9:140728301-140728351	Jurkat	blood:	n/a
15	chr9:140731022-140731072	AG10803	skin:	n/a
16	chr9:140728301-140728351	MCF-7	breast:	n/a
17	chr9:140732731-140732781	SK-N-MC	brain:	n/a
18	chr9:140735058-140735108	Hepatocyte	liver:	n/a
19	chr9:140728491-140728541	MCF10A-Er-Src	breast:	n/a
20	chr9:140732731-140732781	BJ	skin:	n/a
21	chr9:140733714-140733764	NT2-D1	testis:	n/a
22	chr9:140727571-140727621	NB4	blood:	n/a
23	chr9:140732731-140732781	SK-N-SH_RA	brain:	n/a
24	chr9:140738145-140738195	Jurkat	blood:	n/a
25	chr9:140738145-140738195	HAEpiC	amniotic membrane:	n/a
26	chr9:140731445-140731495	GM19239	blood:	n/a
27	chr9:140730317-140730367	HMEC	breast:	n/a
28	chr9:140735359-140735409	CMK	blood:	n/a
29	chr9:140730317-140730367	NHBE	bronchial:	n/a
30	chr9:140731022-140731072	HNPCEpiC	eye:	n/a
31	chr9:140728491-140728541	T-47D	breast:	n/a
32	chr9:140738145-140738195	AG10803	skin:	n/a
33	chr9:140733714-140733764	GM19239	blood:	n/a
34	chr9:140730317-140730367	U87	brain:	n/a
35	chr9:140726863-140726913	GM19239	blood:	n/a
36	chr9:140731445-140731495	SK-N-MC	brain:	n/a
37	chr9:140729712-140729762	SAEC	small airway:	n/a
38	chr9:140731445-140731495	NB4	blood:	n/a
39	chr9:140725898-140725948	NHDF-neo	bronchial:	n/a
40	chr9:140731552-140731602	ProgFib	skin:	n/a
41	chr9:140731445-140731495	GM12891	blood:	n/a
42	chr9:140730317-140730367	Hepatocyte	liver:	n/a
43	chr9:140728491-140728541	SAEC	small airway:	n/a
44	chr9:140729241-140729291	PrEC	prostate:	n/a
45	chr9:140728491-140728541	GM19239	blood:	n/a
46	chr9:140725587-140725637	PFSK-1	brain:	n/a
47	chr9:140733980-140734030	K562	blood:	n/a
48	chr9:140732731-140732781	U87	brain:	n/a
49	chr9:140730806-140730856	SKMC	muscle:	n/a
50	chr9:140728301-140728351	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:140722366..140725361-chr9:140730961..140733725,2	MCF-7	breast:
2	chr9:140720745..140725244-chr9:140725368..140729857,4	K562	blood:
3	chr9:140720128..140722152-chr9:140723312..140725717,2	K562	blood:
4	chr9:140725074..140728358-chr9:140730980..140733506,3	K562	blood:
5	chr9:140732797..140735433-chr9:140735710..140738705,2	MCF-7	breast:
6	chr9:140725074..140728358-chr9:140730980..140733506,3	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-602	chr9:140732886-140732908	MIMAT0003270

No.	miRNA target gene	miRNA name	Chromosome Location
1	EHMT1	hsa-miR-30e-5p	chr9:140730456-140730473
2	EHMT1	hsa-miR-615-3p	chr9:140729903-140729924
3	EHMT1	hsa-miR-1	chr9:140730432-140730455

Variant related genes	Relation type
MIR602	TF binding region
EHMT1	TF binding region
MIR602	CpG island
EHMT1	CpG island
ENSG00000181090	chromatin interactions
ENSG00000207693	chromatin interactions

Extended variants
information (count: 1812 )
Associated
traits (count: 19 )

Variant overlapped rSNPs/rCNVs (count:1812 , 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	rs554962309	chr9:140723512-140723513	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs60972653	chr9:140723557-140723558	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs540044640	chr9:140723565-140723566	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs554505863	chr9:140723566-140723567	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs190243986	chr9:140723577-140723578	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs550092117	chr9:140723598-140723599	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs564748686	chr9:140723682-140723683	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs75268321	chr9:140723760-140723761	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs529558286	chr9:140723775-140723776	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs111987054	chr9:140723786-140723787	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs5029224	chr9:140723799-140723800	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs575321024	chr9:140723846-140723847	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs114563565	chr9:140723852-140723853	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs560576700	chr9:140723866-140723867	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs529636581	chr9:140723884-140723885	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs566091314	chr9:140723903-140723904	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs560025594	chr9:140723945-140723946	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs534985656	chr9:140723951-140723952	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs139128645	chr9:140723952-140723953	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs182457812	chr9:140723956-140723957	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs116551608	chr9:140723977-140723978	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs187923033	chr9:140723978-140723979	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs79714681	chr9:140723997-140723998	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs568515545	chr9:140724008-140724009	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs149875734	chr9:140724030-140724031	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs554168746	chr9:140724041-140724042	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs577615542	chr9:140724048-140724049	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs539718941	chr9:140724103-140724104	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs556733863	chr9:140724155-140724156	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs145432624	chr9:140724178-140724179	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544340416	chr9:140724196-140724197	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376342480	chr9:140724225-140724226	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs560640518	chr9:140724245-140724246	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs574153943	chr9:140724265-140724266	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs553664578	chr9:140724275-140724276	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs559688917	chr9:140724277-140724278	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs192168263	chr9:140724278-140724279	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs370675862	chr9:140724342-140724343	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs537283429	chr9:140724344-140724345	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs552171008	chr9:140724383-140724384	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562733226	chr9:140724387-140724388	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs531403903	chr9:140724410-140724411	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs548743453	chr9:140724422-140724423	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568579605	chr9:140724433-140724434	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs76767385	chr9:140724441-140724442	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs185697909	chr9:140724473-140724474	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs570826751	chr9:140724479-140724480	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs188961423	chr9:140724524-140724525	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs6559231	chr9:140724532-140724533	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs138088940	chr9:140724564-140724565	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:19)

Disease	PMID	Source
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Sudden cardiac death	19188705	CNVD
Myoepithelioma	18604193	CNVD
Tuberous sclerosis	19566914	CNVD
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Mantle cell lymphoma	19029149	CNVD

Chromatin state (count:397 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140711000-140725400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:140712800-140731000	Weak transcription	Psoas Muscle	Psoas
3	chr9:140713000-140728800	Weak transcription	Small Intestine	intestine
4	chr9:140713000-140732200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr9:140713000-140747200	Weak transcription	Stomach Mucosa	stomach
6	chr9:140713600-140733400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr9:140713800-140733200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
8	chr9:140715200-140733800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr9:140716600-140732000	Weak transcription	Fetal Kidney	kidney
10	chr9:140716800-140732800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr9:140718000-140728400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr9:140718000-140732800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr9:140718000-140733200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
14	chr9:140718200-140724400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr9:140718200-140731000	Strong transcription	Fetal Muscle Trunk	muscle
16	chr9:140718200-140732000	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr9:140718400-140724200	Strong transcription	Primary T cells from cord blood	blood
18	chr9:140718400-140724400	Strong transcription	Duodenum Mucosa	Duodenum
19	chr9:140718400-140731800	Strong transcription	Primary T cells fromperipheralblood	blood
20	chr9:140718400-140732000	Strong transcription	Adipose Nuclei	Adipose
21	chr9:140718400-140732200	Strong transcription	Primary T helper cells fromperipheralblood	blood
22	chr9:140718400-140732600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr9:140718600-140724400	Strong transcription	Primary neutrophils fromperipheralblood	blood
24	chr9:140718600-140724400	Strong transcription	Fetal Brain Female	brain
25	chr9:140718600-140731400	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr9:140718600-140732000	Strong transcription	Liver	Liver
27	chr9:140718600-140732400	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr9:140718600-140732600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
29	chr9:140718600-140733400	Strong transcription	Stomach Smooth Muscle	stomach
30	chr9:140718800-140723600	Strong transcription	Colonic Mucosa	Colon
31	chr9:140719200-140727000	Weak transcription	Fetal Heart	heart
32	chr9:140719200-140727400	Strong transcription	Esophagus	oesophagus
33	chr9:140719200-140730000	Weak transcription	NH-A	brain
34	chr9:140719200-140732000	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr9:140719200-140732800	Weak transcription	Fetal Brain Male	brain
36	chr9:140719400-140731800	Weak transcription	K562	blood
37	chr9:140719600-140728200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr9:140719800-140732600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr9:140720000-140723600	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr9:140720000-140727400	Weak transcription	NHDF-Ad	bronchial
41	chr9:140720000-140728600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr9:140720000-140730600	Weak transcription	NHEK	skin
43	chr9:140720000-140732600	Weak transcription	HUVEC	blood vessel
44	chr9:140720200-140732000	Strong transcription	Monocytes-CD14+_RO01746	blood
45	chr9:140720200-140732200	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr9:140720400-140724000	Strong transcription	GM12878-XiMat	blood
47	chr9:140720400-140731800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
48	chr9:140720400-140731800	Strong transcription	Thymus	Thymus
49	chr9:140720400-140732200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr9:140720400-140732200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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