Variant report

Variant	esv20285
Chromosome Location	chr9:139663637-139674967
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	ATF3	chr9:139668076-139668471	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF3	chr9:139668158-139668508	K562	blood:	n/a	n/a
3	ATF3	chr9:139668269-139668395	GM12878	blood:	n/a	n/a
4	ATF3	chr9:139668163-139668543	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF3	chr9:139668130-139668489	GM12878	blood:	n/a	n/a
6	ATF3	chr9:139668215-139668454	HepG2	liver:	n/a	n/a
7	BACH1	chr9:139664383-139664584	H1-hESC	embryonic stem cell:	n/a	n/a
8	BHLHE40	chr9:139664410-139664615	K562	blood:	n/a	n/a
9	BHLHE40	chr9:139664520-139664614	GM12878	blood:	n/a	n/a
10	CBX3	chr9:139664352-139664698	K562	blood:	n/a	n/a
11	CBX3	chr9:139667695-139668588	HCT-116	colon:	n/a	n/a
12	CBX3	chr9:139667717-139668521	K562	blood:	n/a	n/a
13	CBX3	chr9:139667686-139668554	K562	blood:	n/a	n/a
14	CBX3	chr9:139668883-139669223	K562	blood:	n/a	n/a
15	CEBPB	chr9:139664485-139664618	H1-hESC	embryonic stem cell:	n/a	n/a
16	CHD2	chr9:139668218-139668499	K562	blood:	n/a	n/a
17	CHD2	chr9:139664436-139664568	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr9:139668334-139668429	GM12878	blood:	n/a	n/a
19	CHD2	chr9:139668200-139668514	H1-hESC	embryonic stem cell:	n/a	n/a
20	CREB1	chr9:139664368-139664674	A549	lung:	n/a	n/a
21	CTCF	chr9:139674440-139674590	SK-N-SH_RA	brain:	n/a	n/a
22	CTCF	chr9:139664434-139664698	MCF-7	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
23	CTCF	chr9:139674400-139674550	HCM	heart:	n/a	n/a
24	CTCF	chr9:139664500-139664650	HFF-Myc	foreskin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
25	CTCF	chr9:139664328-139664691	MCF-7	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
26	CTCF	chr9:139674333-139674544	HepG2	liver:	n/a	n/a
27	CTCF	chr9:139668260-139668410	BE2_C	brain:	n/a	n/a
28	CTCF	chr9:139664397-139664748	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
29	CTCF	chr9:139664440-139664590	HAc	cerebellar:	n/a	chr9:139664483-139664493 chr9:139664481-139664494
30	CTCF	chr9:139664343-139664685	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
31	CTCF	chr9:139674360-139674510	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr9:139664360-139664510	HFF-Myc	foreskin:	n/a	chr9:139664483-139664493 chr9:139664481-139664494
33	CTCF	chr9:139664462-139664635	T-47D	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
34	CTCF	chr9:139664413-139664738	IMR90	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
35	CTCF	chr9:139664271-139664724	K562	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
36	CTCF	chr9:139674340-139674490	HRE	kidney:	n/a	n/a
37	CTCF	chr9:139664480-139664630	GM06990	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
38	CTCF	chr9:139674400-139674550	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr9:139674420-139674570	AG09319	gingival:	n/a	n/a
40	CTCF	chr9:139674325-139674597	K562	blood:	n/a	n/a
41	CTCF	chr9:139664520-139664670	GM12870	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
42	CTCF	chr9:139664415-139664705	Gliobla	brain:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
43	CTCF	chr9:139664445-139664708	NHEK	skin:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
44	CTCF	chr9:139664480-139664630	HL-60	blood:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
45	CTCF	chr9:139674380-139674530	BE2_C	brain:	n/a	n/a
46	CTCF	chr9:139664500-139664650	HRPEpiC	eye:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
47	CTCF	chr9:139664387-139664709	A549	lung:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664483-139664493 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664481-139664494 chr9:139664588-139664597 chr9:139664585-139664603
48	CTCF	chr9:139674380-139674530	HAc	cerebellar:	n/a	n/a
49	CTCF	chr9:139664500-139664650	MCF-7	breast:	n/a	chr9:139664590-139664600 chr9:139664588-139664601 chr9:139664586-139664602 chr9:139664587-139664608 chr9:139664588-139664597 chr9:139664585-139664603
50	CTCF	chr9:139674300-139674450	NHDF-neo	bronchial:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:139671912..139674656-chr9:140133949..140136932,2	MCF-7	breast:
2	chr9:139671789..139674484-chr9:139759128..139760920,2	MCF-7	breast:
3	chr9:139662310..139665146-chr9:139700169..139702660,2	K562	blood:
4	chr9:139663599..139665182-chr9:139742980..139744994,2	MCF-7	breast:
5	chr9:139662206..139666130-chr9:139666450..139670889,6	K562	blood:
6	chr9:139621278..139624827-chr9:139660350..139665047,5	K562	blood:
7	chr9:139615454..139618647-chr9:139663629..139666598,3	MCF-7	breast:
8	chr9:139662596..139664291-chr9:139666561..139668575,2	K562	blood:
9	chr8:134883443..134884944-chr9:139662718..139664230,2	K562	blood:
10	chr9:139622733..139626444-chr9:139667758..139670003,3	K562	blood:
11	chr9:139662596..139664291-chr9:139666561..139668575,2	K562	blood:
12	chr9:139617845..139623838-chr9:139660350..139667246,10	K562	blood:
13	chr9:139662206..139666130-chr9:139666450..139670889,6	K562	blood:
14	chr9:139640588..139643273-chr9:139662768..139664600,2	K562	blood:
15	chr9:139620940..139622667-chr9:139668115..139669659,2	K562	blood:
16	chr9:139666515..139668281-chr9:139676251..139678403,3	MCF-7	breast:
17	chr9:139663003..139666035-chr9:139678378..139681076,3	MCF-7	breast:
18	chr9:139656220..139657844-chr9:139664541..139666356,2	K562	blood:
19	chr9:139664152..139666690-chr9:139684867..139687116,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM141-1	chr9:139674391-139674670	NONHSAT135598

Variant related genes	Relation type
LCN15	TF binding region
ATP6V1G1P3	TF binding region
ENSG00000267206	chromatin interactions
ENSG00000273066	chromatin interactions
ENSG00000244187	chromatin interactions
ENSG00000107223	chromatin interactions
ENSG00000213213	chromatin interactions
ENSG00000204003	chromatin interactions
ENSG00000233016	chromatin interactions
ENSG00000272896	chromatin interactions
ENSG00000188229	chromatin interactions
ENSG00000196642	chromatin interactions
ENSG00000054148	chromatin interactions

Extended variants
information (count: 496 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:496 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185657477	chr9:139663650-139663651	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
2	rs576135006	chr9:139663670-139663671	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
3	rs542006583	chr9:139663674-139663675	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
4	rs71483290	chr9:139663685-139663686	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs555586040	chr9:139663697-139663698	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs572380895	chr9:139663701-139663702	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs190170158	chr9:139663790-139663791	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs11788335	chr9:139664068-139664069	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs181483657	chr9:139664092-139664093	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
10	rs5021502	chr9:139664100-139664101	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
11	rs71483291	chr9:139664111-139664112	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
12	rs71483292	chr9:139664115-139664116	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
13	rs541397195	chr9:139664119-139664120	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
14	rs564818634	chr9:139664122-139664123	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
15	rs188490507	chr9:139664129-139664130	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
16	rs531986293	chr9:139664135-139664136	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
17	rs545789845	chr9:139664138-139664139	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs200435840	chr9:139664145-139664146	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs374376007	chr9:139664146-139664147	Weak transcription Enhancers	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs112087427	chr9:139664166-139664167	Weak transcription Enhancers	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
21	rs200711553	chr9:139664360-139664361	Active TSS Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
22	rs143180523	chr9:139664402-139664403	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
23	rs76415838	chr9:139664479-139664480	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
24	rs545922049	chr9:139664585-139664586	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
25	rs531476041	chr9:139664595-139664596	Active TSS Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
26	rs548401833	chr9:139664601-139664602	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs200537151	chr9:139664628-139664629	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs568292015	chr9:139664630-139664631	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs200765758	chr9:139664633-139664634	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs181304295	chr9:139664653-139664654	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs527497384	chr9:139664832-139664833	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
32	rs11410546	chr9:139664930-139664931	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs547345031	chr9:139664941-139664942	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs34434890	chr9:139664950-139664951	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs11312933	chr9:139664962-139664963	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs35321281	chr9:139664965-139664966	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs200915792	chr9:139665023-139665024	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs553076854	chr9:139665057-139665058	Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs79790043	chr9:139665091-139665092	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
40	rs148260543	chr9:139665108-139665109	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
41	rs530339448	chr9:139665134-139665135	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
42	rs569809895	chr9:139665136-139665137	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
43	rs140398327	chr9:139665145-139665146	Weak transcription	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
44	rs555527025	chr9:139665249-139665250	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs547241456	chr9:139665283-139665284	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs573230225	chr9:139665288-139665289	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs375991287	chr9:139665296-139665297	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs541635797	chr9:139665309-139665310	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs558124351	chr9:139665316-139665317	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs150340638	chr9:139665322-139665323	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Oral cancer	21386901	CNVD
Cardiac fibroma	18329553	CNVD
Lung cancer	19147751	CNVD
Melanoma	18172304	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Cervical cancer	17311676	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Chordoma	18071362	CNVD
small cell lung cancer	20016488	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Kleefstra Syndrome	21538692	CNVD
Disorders of sex development	22290220	CNVD
Cancer	21183584	CNVD
Chronic myelomonocytic leukemia	16760666	CNVD
Abnormal phenotypes	18644119	CNVD
Ovarian cancer	21720365	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Hepatocellular carcinoma	22174799	CNVD
Idiopathic chronic pancreatitis	21572526	CNVD
Kleefstra syndrome	22670141	CNVD
Schizophrenia	22241247	CNVD
9q deletion syndrome	16826528	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Non-small cell lung cancer	21829676	CNVD
Non-syndromic sensorineural hearing loss	19293338	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Mantle cell lymphoma	19029149	CNVD
Autism	20808228	CNVD
Epilepsy	22083797	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Developmental delay	20877625	CNVD
Hypoplastic	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
Palpebral fissures	20877625	CNVD
Melanoma	20877625	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:159 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:139655600-139664400	Weak transcription	Pancreas	Pancrea
2	chr9:139657600-139664200	Weak transcription	Right Ventricle	heart
3	chr9:139657800-139667800	Weak transcription	Right Atrium	heart
4	chr9:139658400-139664200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:139658400-139664200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr9:139659200-139667800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr9:139661400-139664200	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr9:139662800-139664200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr9:139662800-139664200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr9:139662800-139664200	Weak transcription	HepG2	liver
11	chr9:139662800-139664200	Weak transcription	K562	blood
12	chr9:139662800-139664400	Weak transcription	Fetal Thymus	thymus
13	chr9:139663000-139664200	Weak transcription	Primary B cells from cord blood	blood
14	chr9:139663600-139664000	Weak transcription	Primary B cells from peripheral blood	blood
15	chr9:139664000-139664600	Enhancers	Primary B cells from peripheral blood	blood
16	chr9:139664200-139664400	Active TSS	H1 Cell Line	embryonic stem cell
17	chr9:139664200-139664400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
18	chr9:139664200-139664400	Enhancers	Primary B cells from cord blood	blood
19	chr9:139664200-139664400	Enhancers	Primary hematopoietic stem cells	blood
20	chr9:139664200-139664400	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
21	chr9:139664200-139664400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr9:139664200-139664400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr9:139664200-139664400	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr9:139664200-139664400	Active TSS	Rectal Mucosa Donor 31	rectum
25	chr9:139664200-139664600	Active TSS	ES-I3 Cell Line	embryonic stem cell
26	chr9:139664200-139664600	Active TSS	H9 Cell Line	embryonic stem cell
27	chr9:139664200-139664600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr9:139664200-139664600	Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr9:139664200-139664600	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr9:139664200-139664600	Active TSS	HUES64 Cell Line	embryonic stem cell
31	chr9:139664200-139664600	Active TSS	iPS-15b Cell Line	embryonic stem cell
32	chr9:139664200-139664600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr9:139664200-139664600	Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr9:139664200-139664600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr9:139664200-139664600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr9:139664200-139664600	Enhancers	Primary T cells from cord blood	blood
37	chr9:139664200-139664600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
38	chr9:139664200-139664600	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr9:139664200-139664600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr9:139664200-139664600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
41	chr9:139664200-139664600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
42	chr9:139664200-139664600	Enhancers	Primary T helper cells fromperipheralblood	blood
43	chr9:139664200-139664600	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
44	chr9:139664200-139664600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
45	chr9:139664200-139664600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr9:139664200-139664600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr9:139664200-139664600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
48	chr9:139664200-139664600	Enhancers	Fetal Intestine Large	intestine
49	chr9:139664200-139664600	Enhancers	Fetal Intestine Small	intestine
50	chr9:139664200-139664600	Bivalent Enhancer	Fetal Muscle Trunk	muscle

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