Variant report

Variant	nsv525830
Chromosome Location	chr4:9451923-9599790
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	chr4:9454189-9454353	HepG2	liver:	n/a	n/a
2	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
4	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
5	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
6	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
7	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
8	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
9	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
10	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
11	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
12	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
13	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
15	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:9533811-9533913	K562	blood:	n/a	n/a
17	CBX3	chr4:9597420-9597667	K562	blood:	n/a	n/a
18	CCNT2	chr4:9533734-9533999	K562	blood:	n/a	n/a
19	CEBPB	chr4:9530664-9530884	K562	blood:	n/a	n/a
20	CEBPB	chr4:9596784-9597029	HepG2	liver:	n/a	chr4:9596883-9596894
21	CEBPB	chr4:9531399-9531602	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:9453481-9453664	HepG2	liver:	n/a	chr4:9453618-9453629
23	CEBPB	chr4:9530595-9530856	K562	blood:	n/a	n/a
24	CEBPB	chr4:9585906-9586106	HepG2	liver:	n/a	chr4:9585991-9586002
25	CEBPB	chr4:9530676-9530843	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr4:9533998-9534198	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr4:9533893-9534015	HepG2	liver:	n/a	chr4:9533994-9534004
28	CHD2	chr4:9533949-9534111	H1-hESC	embryonic stem cell:	n/a	chr4:9533994-9534004
29	CTCF	chr4:9497176-9497409	MCF-7	breast:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
30	CTCF	chr4:9533780-9533930	GM12873	blood:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
31	CTCF	chr4:9579600-9579750	GM12872	blood:	n/a	n/a
32	CTCF	chr4:9546150-9546359	H1-hESC	embryonic stem cell:	n/a	chr4:9546245-9546261 chr4:9546244-9546262 chr4:9546239-9546260
33	CTCF	chr4:9497200-9497350	Hela-S3	cervix:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
34	CTCF	chr4:9479426-9479509	GM13976	blood:	n/a	n/a
35	CTCF	chr4:9533763-9534037	T-47D	breast:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
36	CTCF	chr4:9497200-9497350	HEK293	kidney:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
37	CTCF	chr4:9497200-9497350	K562	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
38	CTCF	chr4:9496975-9497007	LNCaP	prostate:	n/a	n/a
39	CTCF	chr4:9497200-9497350	GM12864	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
40	CTCF	chr4:9497200-9497350	GM12875	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
41	CTCF	chr4:9546088-9546358	A549	lung:	n/a	chr4:9546245-9546261 chr4:9546244-9546262 chr4:9546239-9546260
42	CTCF	chr4:9546143-9546284	GM12892	blood:	n/a	chr4:9546245-9546261 chr4:9546244-9546262 chr4:9546239-9546260
43	CTCF	chr4:9546131-9546279	MCF-7	breast:	n/a	chr4:9546245-9546261 chr4:9546244-9546262 chr4:9546239-9546260
44	CTCF	chr4:9585583-9585633	GM10248	blood:	n/a	n/a
45	CTCF	chr4:9533780-9533930	AG04449	skin:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
46	CTCF	chr4:9533840-9533990	AG10803	skin:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884
47	CTCF	chr4:9497200-9497350	HUVEC	blood vessel:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
48	CTCF	chr4:9546136-9546281	MCF-7	breast:	n/a	chr4:9546245-9546261 chr4:9546244-9546262 chr4:9546239-9546260
49	CTCF	chr4:9497240-9497390	GM12867	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
50	CTCF	chr4:9533717-9534017	MCF-7	breast:	n/a	chr4:9533869-9533890 chr4:9533870-9533883 chr4:9533867-9533885 chr4:9533870-9533883 chr4:9533891-9533904 chr4:9533868-9533884

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9494487-9494537	HRE	kidney:	n/a
2	chr4:9481822-9481872	SK-N-SH	brain:	n/a
3	chr4:9506681-9506731	HMEC	breast:	n/a
4	chr4:9494487-9494537	HRE	kidney:	n/a
5	chr4:9481822-9481872	SK-N-SH	brain:	n/a
6	chr4:9506681-9506731	HMEC	breast:	n/a
7	chr4:9499367-9499417	HRE	kidney:	n/a
8	chr4:9523635-9523685	HRE	kidney:	n/a
9	chr4:9484735-9484785	AG10803	skin:	n/a
10	chr4:9509896-9509946	K562	blood:	n/a
11	chr4:9485487-9485537	HCM	heart:	n/a
12	chr4:9523635-9523685	A549	lung:	n/a
13	chr4:9505764-9505814	NT2-D1	testis:	n/a
14	chr4:9509830-9509880	GM12878	blood:	n/a
15	chr4:9508890-9508940	Caco-2	colon:	n/a
16	chr4:9505698-9505748	HepG2	liver:	n/a
17	chr4:9508240-9508290	HRPEpiC	eye:	n/a
18	chr4:9523653-9523703	U87	brain:	n/a
19	chr4:9482233-9482283	NH-A	brain:	n/a
20	chr4:9523653-9523703	HCF	heart:	n/a
21	chr4:9510844-9510894	PrEC	prostate:	n/a
22	chr4:9482074-9482124	NB4	blood:	n/a
23	chr4:9500174-9500224	HL-60	blood:	n/a
24	chr4:9534388-9534438	PrEC	prostate:	n/a
25	chr4:9503404-9503454	HRE	kidney:	n/a
26	chr4:9533205-9533255	AG09309	skin:	n/a
27	chr4:9507499-9507549	GM12878	blood:	n/a
28	chr4:9481822-9481872	AG10803	skin:	n/a
29	chr4:9534366-9534416	HRE	kidney:	n/a
30	chr4:9457537-9457587	PFSK-1	brain:	n/a
31	chr4:9523635-9523685	ovcar-3	ovarian:	n/a
32	chr4:9505764-9505814	HRCEpiC	kidney:	n/a
33	chr4:9481822-9481872	ECC-1	luminal epithelium:	n/a
34	chr4:9509787-9509837	K562	blood:	n/a
35	chr4:9507285-9507335	HNPCEpiC	eye:	n/a
36	chr4:9557805-9557855	HEEpiC	esophagus:	n/a
37	chr4:9510286-9510336	ECC-1	luminal epithelium:	n/a
38	chr4:9508890-9508940	GM12878	blood:	n/a
39	chr4:9495454-9495504	BJ	skin:	n/a
40	chr4:9507285-9507335	U87	brain:	n/a
41	chr4:9533426-9533476	RPTEC	kidney:	n/a
42	chr4:9558893-9558943	SK-N-MC	brain:	n/a
43	chr4:9492758-9492808	GM06990	blood:	n/a
44	chr4:9493231-9493281	HCM	heart:	n/a
45	chr4:9493536-9493586	ProgFib	skin:	n/a
46	chr4:9481822-9481872	PrEC	prostate:	n/a
47	chr4:9537404-9537454	SKMC	muscle:	n/a
48	chr4:9534388-9534438	HRE	kidney:	n/a
49	chr4:9495454-9495504	HEEpiC	esophagus:	n/a
50	chr4:9506681-9506731	MCF-7	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:
2	chr4:9533415..9534346-chr4:9660887..9661684,2	MCF-7	breast:
3	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-1396O13.13.1-3	chr4:9555234-9555605	NONHSAT095137
2	lnc-DEFB131-1	chr4:9470746-9471694	NONHSAT095133

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548i	chr4:9557878-9557899	MIMAT0005935_1

Variant related genes	Relation type
OR7E85P	TF binding region
ENSG00000266246	TF binding region
ENSG00000249799	TF binding region
OR7E84P	TF binding region
OR7E86P	TF binding region
MIR548I2	TF binding region
ENSG00000249443	TF binding region
UNC93B7	TF binding region
OR7E83P	TF binding region
ENSG00000242034	TF binding region
ENSG00000244004	TF binding region
OR7E85P	CpG island
ENSG00000266246	CpG island
ENSG00000249799	CpG island
OR7E84P	CpG island
OR7E86P	CpG island
MIR548I2	CpG island
ENSG00000249443	CpG island
UNC93B7	CpG island
OR7E83P	CpG island
ENSG00000242034	CpG island
ENSG00000244004	CpG island

Extended variants
information (count: 8506 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:8506 , 50 per page) page: 1 2 3 4 5 6 7 ... 171

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537410607	chr4:9452609-9452610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs6844838	chr4:9452616-9452617	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs374375700	chr4:9452633-9452634	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569142784	chr4:9452636-9452637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs368860322	chr4:9452654-9452655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539847520	chr4:9452659-9452660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557751217	chr4:9452677-9452678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs114632096	chr4:9452703-9452704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534036878	chr4:9452714-9452715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555491475	chr4:9452715-9452716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574219430	chr4:9452717-9452718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544566260	chr4:9452724-9452725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs556848457	chr4:9452725-9452726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs6849780	chr4:9452734-9452735	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs544765009	chr4:9452743-9452744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79170033	chr4:9452749-9452750	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs185095772	chr4:9452758-9452759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574808314	chr4:9452779-9452780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527336851	chr4:9452797-9452798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541396307	chr4:9452808-9452809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111302495	chr4:9452810-9452811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs189219906	chr4:9452822-9452823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs545922485	chr4:9452829-9452830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181620289	chr4:9452832-9452833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs549786881	chr4:9452849-9452850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140452798	chr4:9452876-9452877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377498261	chr4:9452887-9452888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs553539978	chr4:9452890-9452891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs10011737	chr4:9452894-9452895	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs6856153	chr4:9452898-9452899	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs183977421	chr4:9452900-9452901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs540306373	chr4:9452909-9452910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566531219	chr4:9452917-9452918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534023370	chr4:9452928-9452929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188756038	chr4:9452930-9452931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567741021	chr4:9452934-9452935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs6850194	chr4:9452936-9452937	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs111879603	chr4:9452953-9452954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs529303827	chr4:9452959-9452960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs186217911	chr4:9452973-9452974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs11935532	chr4:9452974-9452975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544233867	chr4:9452978-9452979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs561932784	chr4:9452979-9452980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs553799455	chr4:9452982-9452983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs572114999	chr4:9452993-9452994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs542731062	chr4:9453000-9453001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561067952	chr4:9453010-9453011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs191891649	chr4:9453025-9453026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs543567502	chr4:9453030-9453031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs10011866	chr4:9453032-9453033	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:58)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9452600-9453800	Enhancers	Small Intestine	intestine
2	chr4:9453000-9453800	Enhancers	Duodenum Mucosa	Duodenum
3	chr4:9453600-9454800	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr4:9453600-9456200	Enhancers	Fetal Intestine Large	intestine
5	chr4:9453600-9456800	Enhancers	Fetal Intestine Small	intestine
6	chr4:9453600-9457200	Enhancers	Stomach Mucosa	stomach
7	chr4:9453800-9454600	Weak transcription	Duodenum Mucosa	Duodenum
8	chr4:9454600-9454800	Enhancers	Duodenum Mucosa	Duodenum
9	chr4:9454800-9455200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr4:9454800-9455800	Weak transcription	Rectal Mucosa Donor 31	rectum
11	chr4:9455200-9457200	Enhancers	Duodenum Mucosa	Duodenum
12	chr4:9455800-9456800	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:9455800-9457200	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr4:9456400-9456800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:9456400-9457200	Enhancers	Gastric	stomach
16	chr4:9476200-9477000	Bivalent Enhancer	Fetal Brain Male	brain
17	chr4:9476600-9477000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
18	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
19	chr4:9476600-9477000	Bivalent Enhancer	Fetal Muscle Leg	muscle
20	chr4:9477000-9477400	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr4:9481600-9482000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:9481600-9482000	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr4:9481800-9482000	Enhancers	Duodenum Mucosa	Duodenum
24	chr4:9484800-9503800	Weak transcription	Right Atrium	heart
25	chr4:9495800-9496800	Enhancers	Fetal Thymus	thymus
26	chr4:9496200-9496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr4:9496200-9496800	Enhancers	Thymus	Thymus
28	chr4:9496200-9497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr4:9496400-9496600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr4:9496400-9496800	Enhancers	Primary hematopoietic stem cells	blood
31	chr4:9496600-9499000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:9496800-9499600	Weak transcription	Primary hematopoietic stem cells	blood
33	chr4:9499000-9499200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
34	chr4:9499000-9499200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
35	chr4:9499000-9499600	Enhancers	Liver	Liver
36	chr4:9499000-9500400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
37	chr4:9499000-9500600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr4:9499200-9499400	Bivalent Enhancer	Fetal Thymus	thymus
39	chr4:9499200-9499600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr4:9499200-9499800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr4:9499200-9499800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
42	chr4:9499200-9500200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
43	chr4:9499200-9500200	Bivalent Enhancer	Adipose Nuclei	Adipose
44	chr4:9499200-9500400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
45	chr4:9499200-9500400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr4:9499200-9500600	Active TSS	H9 Cell Line	embryonic stem cell
47	chr4:9499200-9500600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
48	chr4:9499200-9500600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
49	chr4:9499200-9500600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
50	chr4:9499200-9500600	Active TSS	Breast Myoepithelial Primary Cells	Breast

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links