Variant report

Variant	esv3372704
Chromosome Location	chr9:140498156-140501504
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:476)
CpG islands
(count:488)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr9:140500314-140500576	K562	blood:	n/a	n/a
2	ATF3	chr9:140499555-140499816	K562	blood:	n/a	chr9:140499631-140499640
3	BHLHE40	chr9:140500196-140500599	K562	blood:	n/a	chr9:140500319-140500335
4	BHLHE40	chr9:140499598-140499770	GM12878	blood:	n/a	n/a
5	BHLHE40	chr9:140499614-140499783	HepG2	liver:	n/a	n/a
6	BHLHE40	chr9:140499561-140499836	K562	blood:	n/a	n/a
7	BHLHE40	chr9:140500257-140500479	GM12878	blood:	n/a	chr9:140500319-140500335
8	CCNT2	chr9:140500097-140500918	K562	blood:	n/a	n/a
9	CCNT2	chr9:140499584-140499771	K562	blood:	n/a	chr9:140499637-140499646 chr9:140499631-140499640
10	CEBPB	chr9:140500560-140501005	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr9:140500278-140500292	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr9:140500713-140500961	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr9:140499663-140499773	Hela-S3	cervix:	n/a	n/a
14	CEBPD	chr9:140500070-140500305	HepG2	liver:	n/a	n/a
15	CEBPD	chr9:140500087-140500279	HepG2	liver:	n/a	n/a
16	CHD1	chr9:140500518-140500542	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr9:140500172-140500390	GM12878	blood:	n/a	n/a
18	CHD2	chr9:140499603-140499785	GM12878	blood:	n/a	n/a
19	CHD2	chr9:140500205-140500356	HepG2	liver:	n/a	n/a
20	CHD2	chr9:140499626-140499628	K562	blood:	n/a	n/a
21	CHD2	chr9:140500526-140500554	K562	blood:	n/a	n/a
22	CHD2	chr9:140499356-140501075	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr9:140499635-140499748	H1-hESC	embryonic stem cell:	n/a	n/a
24	CREB1	chr9:140499561-140499826	ECC-1	luminal epithelium:	n/a	n/a
25	CREB1	chr9:140499409-140500377	GM12878	blood:	n/a	n/a
26	CREB1	chr9:140499402-140499916	K562	blood:	n/a	n/a
27	CREB1	chr9:140499418-140499904	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr9:140499423-140499860	A549	lung:	n/a	n/a
29	CREB1	chr9:140499393-140499927	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr9:140499420-140500497	HepG2	liver:	n/a	n/a
31	CREB1	chr9:140500506-140500843	A549	lung:	n/a	n/a
32	CTCF	chr9:140500125-140500227	GM19239	blood:	n/a	n/a
33	CTCF	chr9:140500760-140500910	GM12872	blood:	n/a	n/a
34	CTCF	chr9:140500707-140500713	MCF-7	breast:	n/a	n/a
35	CTCF	chr9:140500495-140500496	GM10248	blood:	n/a	n/a
36	CTCF	chr9:140499645-140499772	MCF-7	breast:	n/a	n/a
37	CTCF	chr9:140499655-140499759	GM19240	blood:	n/a	n/a
38	CTCF	chr9:140499599-140499806	GM12878	blood:	n/a	n/a
39	CTCF	chr9:140499646-140499760	GM19238	blood:	n/a	n/a
40	CTCF	chr9:140500146-140500226	Lung_OC	lung:	n/a	n/a
41	CTCF	chr9:140500693-140500819	GM12891	blood:	n/a	chr9:140500719-140500732
42	CTCF	chr9:140499628-140499774	Spleen_OC	spleen:	n/a	n/a
43	CTCF	chr9:140499642-140499774	GM12892	blood:	n/a	n/a
44	CTCF	chr9:140500131-140500190	NHEK	skin:	n/a	n/a
45	CTCF	chr9:140500152-140500217	MCF-7	breast:	n/a	n/a
46	CTCF	chr9:140499698-140499744	GM12891	blood:	n/a	n/a
47	CTCF	chr9:140499623-140499625	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr9:140500173-140500250	GM19238	blood:	n/a	n/a
49	CTCF	chr9:140499617-140499769	K562	blood:	n/a	n/a
50	CTCF	chr9:140499580-140499730	HMEC	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:140500813-140500863	Caco-2	colon:	n/a
2	chr9:140499132-140499182	SK-N-SH	brain:	n/a
3	chr9:140500037-140500087	NHDF-neo	bronchial:	n/a
4	chr9:140500037-140500087	HCM	heart:	n/a
5	chr9:140499397-140499447	HEEpiC	esophagus:	n/a
6	chr9:140499623-140499673	Hepatocyte	liver:	n/a
7	chr9:140500208-140500258	GM12878	blood:	n/a
8	chr9:140501305-140501355	MCF10A-Er-Src	breast:	n/a
9	chr9:140500037-140500087	HRE	kidney:	n/a
10	chr9:140499397-140499447	MCF-7	breast:	n/a
11	chr9:140499623-140499673	NHBE	bronchial:	n/a
12	chr9:140501305-140501355	HIPEpiC	eye:	n/a
13	chr9:140500813-140500863	HPAEpiC	pulmonary alveolar:	n/a
14	chr9:140500208-140500258	HCM	heart:	n/a
15	chr9:140500813-140500863	GM19239	blood:	n/a
16	chr9:140500208-140500258	HCT-116	colon:	n/a
17	chr9:140500208-140500258	H1-hESC	embryonic stem cell:	embryo
18	chr9:140499623-140499673	HCF	heart:	n/a
19	chr9:140499132-140499182	SKMC	muscle:	n/a
20	chr9:140500680-140500730	Jurkat	blood:	n/a
21	chr9:140500037-140500087	HNPCEpiC	eye:	n/a
22	chr9:140500813-140500863	GM12878	blood:	n/a
23	chr9:140501305-140501355	GM12878	blood:	n/a
24	chr9:140499397-140499447	LNCaP	prostate:	n/a
25	chr9:140500813-140500863	NHBE	bronchial:	n/a
26	chr9:140500813-140500863	AG04449	skin:	fetal
27	chr9:140500037-140500087	GM12878	blood:	n/a
28	chr9:140500208-140500258	AoSMC	blood vessel:	n/a
29	chr9:140500680-140500730	SK-N-MC	brain:	n/a
30	chr9:140500680-140500730	MCF10A-Er-Src	breast:	n/a
31	chr9:140500037-140500087	HCT-116	colon:	n/a
32	chr9:140500037-140500087	SK-N-MC	brain:	n/a
33	chr9:140499397-140499447	SAEC	small airway:	n/a
34	chr9:140500813-140500863	ovcar-3	ovarian:	n/a
35	chr9:140500680-140500730	BE2_C	brain:	n/a
36	chr9:140499132-140499182	HMEC	breast:	n/a
37	chr9:140499132-140499182	Hela-S3	cervix:	n/a
38	chr9:140499623-140499673	PFSK-1	brain:	n/a
39	chr9:140500680-140500730	GM06990	blood:	n/a
40	chr9:140499623-140499673	K562	blood:	n/a
41	chr9:140500208-140500258	Caco-2	colon:	n/a
42	chr9:140501305-140501355	NHBE	bronchial:	n/a
43	chr9:140500208-140500258	ECC-1	luminal epithelium:	n/a
44	chr9:140500813-140500863	ECC-1	luminal epithelium:	n/a
45	chr9:140500680-140500730	H1-hESC	embryonic stem cell:	embryo
46	chr9:140499132-140499182	AG04450	lung:	fetal
47	chr9:140500037-140500087	BE2_C	brain:	n/a
48	chr9:140499623-140499673	HUVEC	blood vessel:	n/a
49	chr9:140500813-140500863	HRPEpiC	eye:	n/a
50	chr9:140501305-140501355	GM19239	blood:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:140447049..140448753-chr9:140497892..140500070,2	K562	blood:
2	chr9:140470445..140476327-chr9:140498022..140503450,9	K562	blood:
3	chr17:56707742..56709303-chr9:140500647..140503505,2	MCF-7	breast:
4	chr9:140443433..140448155-chr9:140497818..140502870,8	MCF-7	breast:
5	chr9:140482616..140489091-chr9:140495925..140503345,17	MCF-7	breast:
6	chr2:219433435..219434245-chr9:140499709..140500590,2	Hela-S3	cervix:
7	chr9:140443479..140444983-chr9:140499290..140501657,2	K562	blood:
8	chr9:140477211..140479524-chr9:140496943..140498868,3	K562	blood:
9	chr5:108745145..108746117-chr9:140500319..140500843,2	Hela-S3	cervix:
10	chr9:140480405..140490432-chr9:140494944..140502746,26	K562	blood:
11	chr9:140500723..140503070-chr9:140566116..140568927,3	K562	blood:
12	chr9:140470600..140473358-chr9:140498484..140501413,2	K562	blood:
13	chr9:140470766..140479486-chr9:140497266..140502997,13	MCF-7	breast:
14	chr9:140444986..140448753-chr9:140497892..140501428,4	K562	blood:
15	chr9:140491452..140494377-chr9:140498511..140500095,2	K562	blood:
16	chr9:140482416..140489757-chr9:140495738..140502746,21	K562	blood:
17	chr9:140353049..140355083-chr9:140500607..140502657,2	K562	blood:
18	chr9:140498043..140499599-chr9:140558636..140561270,2	MCF-7	breast:
19	chr9:140444055..140447780-chr9:140498087..140502451,7	MCF-7	breast:

No data

Variant related genes	Relation type
ARRDC1	TF binding region
ARRDC1	CpG island
ENSG00000198961	chromatin interactions
ENSG00000144580	chromatin interactions
ENSG00000182154	chromatin interactions
ENSG00000165802	chromatin interactions
ENSG00000148399	chromatin interactions
ENSG00000165724	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000130653	chromatin interactions

Extended variants
information (count: 112 )
Associated
traits (count: 20 )

Variant overlapped rSNPs/rCNVs (count:112 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566583718	chr9:140498165-140498166	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs12341344	chr9:140498172-140498173	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs552198124	chr9:140498175-140498176	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs562382242	chr9:140498176-140498177	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs184875675	chr9:140498190-140498191	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs139166615	chr9:140498203-140498204	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs117552873	chr9:140498230-140498231	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs548731055	chr9:140498233-140498234	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs144711688	chr9:140498234-140498235	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs575521209	chr9:140498242-140498243	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs189336833	chr9:140498245-140498246	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs553043142	chr9:140498246-140498247	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs547284705	chr9:140498255-140498256	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs570580185	chr9:140498256-140498257	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs545122531	chr9:140498263-140498264	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs369598015	chr9:140498266-140498267	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs564901875	chr9:140498320-140498321	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs74568194	chr9:140498333-140498334	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs544513324	chr9:140498341-140498342	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs544597249	chr9:140498346-140498347	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs560998812	chr9:140498351-140498352	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs529903929	chr9:140498357-140498358	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs546516093	chr9:140498381-140498382	Weak transcription Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs559910757	chr9:140498390-140498391	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs532495518	chr9:140498395-140498396	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs12684680	chr9:140498397-140498398	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs552234961	chr9:140498408-140498409	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs72765180	chr9:140498452-140498453	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs369400465	chr9:140498566-140498567	Bivalent Enhancer Weak transcription Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs147878782	chr9:140498623-140498624	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs568619089	chr9:140498625-140498626	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs77289485	chr9:140498628-140498629	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs111406490	chr9:140498643-140498644	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs554454748	chr9:140498696-140498697	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs571036665	chr9:140498704-140498705	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs538775878	chr9:140498751-140498752	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs558654590	chr9:140498756-140498757	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs11789062	chr9:140498789-140498790	Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs575335878	chr9:140498807-140498808	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs199504678	chr9:140498810-140498811	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs180804100	chr9:140498845-140498846	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs554538296	chr9:140498920-140498921	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs574687910	chr9:140498944-140498945	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs540496005	chr9:140498984-140498985	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs575666389	chr9:140499019-140499020	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs559947469	chr9:140499024-140499025	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs141494141	chr9:140499027-140499028	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs185021942	chr9:140499044-140499045	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs562595193	chr9:140499062-140499063	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs72765181	chr9:140499072-140499073	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:20)

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
Breast cancer	21509527	CNVD

Chromatin state (count:500 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:140485800-140499000	Weak transcription	Right Atrium	heart
2	chr9:140485800-140499000	Weak transcription	Stomach Smooth Muscle	stomach
3	chr9:140486200-140498600	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr9:140487400-140498400	Weak transcription	Esophagus	oesophagus
5	chr9:140493200-140498600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:140493400-140498800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr9:140493400-140499000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr9:140493400-140499000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr9:140493400-140499000	Weak transcription	Gastric	stomach
10	chr9:140493600-140498400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr9:140493600-140499000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr9:140496400-140498200	Enhancers	Primary B cells from cord blood	blood
13	chr9:140496400-140498800	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr9:140496400-140498800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr9:140496400-140499400	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr9:140496600-140499000	Enhancers	K562	blood
17	chr9:140497000-140498800	Enhancers	Primary hematopoietic stem cells	blood
18	chr9:140497000-140499000	Enhancers	Brain Anterior Caudate	brain
19	chr9:140497200-140498200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
20	chr9:140497400-140498400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
21	chr9:140497400-140498800	Weak transcription	A549	lung
22	chr9:140497400-140499000	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr9:140497400-140499400	Enhancers	Spleen	Spleen
24	chr9:140497600-140498600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr9:140497600-140498600	Weak transcription	Adipose Nuclei	Adipose
26	chr9:140497600-140498600	Weak transcription	Fetal Thymus	thymus
27	chr9:140497600-140499000	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr9:140497600-140499600	Weak transcription	Brain Substantia Nigra	brain
29	chr9:140497600-140500200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr9:140497800-140498600	Weak transcription	Hela-S3	cervix
31	chr9:140497800-140498800	Weak transcription	Primary B cells from peripheral blood	blood
32	chr9:140497800-140498800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr9:140497800-140498800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr9:140497800-140498800	Enhancers	Brain Angular Gyrus	brain
35	chr9:140497800-140499000	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr9:140498000-140498600	Weak transcription	Brain Hippocampus Middle	brain
37	chr9:140498000-140498800	Weak transcription	Brain Cingulate Gyrus	brain
38	chr9:140498000-140499000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr9:140498000-140499000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr9:140498000-140499600	Enhancers	Skeletal Muscle Female	skeletal muscle
41	chr9:140498000-140500000	Weak transcription	Primary neutrophils fromperipheralblood	blood
42	chr9:140498200-140498600	Weak transcription	Primary B cells from cord blood	blood
43	chr9:140498200-140498600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr9:140498400-140498600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
45	chr9:140498400-140498600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr9:140498400-140498600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr9:140498400-140498600	Enhancers	Psoas Muscle	Psoas
48	chr9:140498400-140498600	Bivalent Enhancer	HepG2	liver
49	chr9:140498400-140498800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr9:140498400-140498800	Enhancers	Esophagus	oesophagus

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