Variant report

Variant	nsv1000308
Chromosome Location	chr4:9496282-9674336
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1278)
CpG islands
(count:3363)
Chromatin interactive
region (count:4)
LncRNA
region (count:1)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1278 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:9533750-9534097	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:9605857-9606056	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:9547853-9548038	GM12878	blood:	n/a	n/a
4	BATF	chr4:9560693-9560899	GM12878	blood:	n/a	n/a
5	BATF	chr4:9582818-9583030	GM12878	blood:	n/a	n/a
6	BATF	chr4:9605704-9606128	GM12878	blood:	n/a	n/a
7	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
8	BATF	chr4:9606281-9606749	GM12878	blood:	n/a	n/a
9	BATF	chr4:9661377-9661663	GM12878	blood:	n/a	n/a
10	BATF	chr4:9560631-9560870	GM12878	blood:	n/a	n/a
11	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
12	BATF	chr4:9606359-9606745	GM12878	blood:	n/a	n/a
13	BATF	chr4:9609959-9610276	GM12878	blood:	n/a	n/a
14	BATF	chr4:9609924-9610228	GM12878	blood:	n/a	n/a
15	BATF	chr4:9637521-9637725	GM12878	blood:	n/a	n/a
16	BATF	chr4:9582796-9583040	GM12878	blood:	n/a	n/a
17	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
18	BATF	chr4:9661312-9661676	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:9609970-9610277	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:9605814-9606174	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:9637557-9637806	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:9606478-9606683	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:9609991-9610319	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:9547498-9547747	GM12878	blood:	n/a	n/a
25	BCL11A	chr4:9606348-9606693	GM12878	blood:	n/a	n/a
26	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
27	BCL11A	chr4:9605779-9606088	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:9661303-9661712	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:9661297-9661608	HepG2	liver:	n/a	n/a
30	BHLHE40	chr4:9533811-9533913	K562	blood:	n/a	n/a
31	CBX3	chr4:9597420-9597667	K562	blood:	n/a	n/a
32	CCNT2	chr4:9533734-9533999	K562	blood:	n/a	n/a
33	CEBPB	chr4:9605743-9605929	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:9530595-9530856	K562	blood:	n/a	n/a
35	CEBPB	chr4:9585906-9586106	HepG2	liver:	n/a	chr4:9585991-9586002
36	CEBPB	chr4:9596784-9597029	HepG2	liver:	n/a	chr4:9596883-9596894
37	CEBPB	chr4:9639784-9639891	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:9600979-9601222	K562	blood:	n/a	n/a
39	CEBPB	chr4:9531399-9531602	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr4:9661262-9661447	K562	blood:	n/a	n/a
41	CEBPB	chr4:9637488-9637693	HepG2	liver:	n/a	chr4:9637617-9637628
42	CEBPB	chr4:9608408-9608590	K562	blood:	n/a	n/a
43	CEBPB	chr4:9629876-9630149	HepG2	liver:	n/a	chr4:9630037-9630048
44	CEBPB	chr4:9530664-9530884	K562	blood:	n/a	n/a
45	CEBPB	chr4:9530676-9530843	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPD	chr4:9608329-9608642	K562	blood:	n/a	n/a
47	CHD1	chr4:9613391-9613550	GM12878	blood:	n/a	n/a
48	CHD1	chr4:9533998-9534198	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr4:9533893-9534015	HepG2	liver:	n/a	chr4:9533994-9534004
50	CHD2	chr4:9533949-9534111	H1-hESC	embryonic stem cell:	n/a	chr4:9533994-9534004

(count:3363 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9509830-9509880	GM12891	blood:	n/a
2	chr4:9558893-9558943	HRE	kidney:	n/a
3	chr4:9510286-9510336	T-47D	breast:	n/a
4	chr4:9601996-9602046	HCT-116	colon:	n/a
5	chr4:9533948-9533998	K562	blood:	n/a
6	chr4:9523635-9523685	CMK	blood:	n/a
7	chr4:9601996-9602046	NH-A	brain:	n/a
8	chr4:9500174-9500224	H1-hESC	embryonic stem cell:	embryo
9	chr4:9509830-9509880	GM12891	blood:	n/a
10	chr4:9558893-9558943	HRE	kidney:	n/a
11	chr4:9510286-9510336	T-47D	breast:	n/a
12	chr4:9601996-9602046	HCT-116	colon:	n/a
13	chr4:9533948-9533998	K562	blood:	n/a
14	chr4:9523635-9523685	CMK	blood:	n/a
15	chr4:9601996-9602046	NH-A	brain:	n/a
16	chr4:9500174-9500224	H1-hESC	embryonic stem cell:	embryo
17	chr4:9507499-9507549	Hela-S3	cervix:	n/a
18	chr4:9602138-9602188	HIPEpiC	eye:	n/a
19	chr4:9661422-9661472	MCF10A-Er-Src	breast:	n/a
20	chr4:9604340-9604390	SK-N-MC	brain:	n/a
21	chr4:9534366-9534416	HepG2	liver:	n/a
22	chr4:9510572-9510622	SK-N-SH_RA	brain:	n/a
23	chr4:9558753-9558803	GM12892	blood:	n/a
24	chr4:9508254-9508304	HRPEpiC	eye:	n/a
25	chr4:9601996-9602046	HEEpiC	esophagus:	n/a
26	chr4:9534062-9534112	NHBE	bronchial:	n/a
27	chr4:9505764-9505814	CMK	blood:	n/a
28	chr4:9558753-9558803	ProgFib	skin:	n/a
29	chr4:9604780-9604830	HUVEC	blood vessel:	n/a
30	chr4:9508890-9508940	LNCaP	prostate:	n/a
31	chr4:9661422-9661472	HepG2	liver:	n/a
32	chr4:9508177-9508227	Jurkat	blood:	n/a
33	chr4:9500174-9500224	HRCEpiC	kidney:	n/a
34	chr4:9508177-9508227	Hela-S3	cervix:	n/a
35	chr4:9534366-9534416	NH-A	brain:	n/a
36	chr4:9499878-9499928	SK-N-SH_RA	brain:	n/a
37	chr4:9509896-9509946	SK-N-SH	brain:	n/a
38	chr4:9508240-9508290	BE2_C	brain:	n/a
39	chr4:9604187-9604237	HIPEpiC	eye:	n/a
40	chr4:9505191-9505241	NB4	blood:	n/a
41	chr4:9510286-9510336	SK-N-SH	brain:	n/a
42	chr4:9514840-9514890	HEK293	kidney:	embryo
43	chr4:9558753-9558803	HIPEpiC	eye:	n/a
44	chr4:9602138-9602188	HepG2	liver:	n/a
45	chr4:9508890-9508940	AG10803	skin:	n/a
46	chr4:9507499-9507549	SKMC	muscle:	n/a
47	chr4:9604187-9604237	HL-60	blood:	n/a
48	chr4:9510572-9510622	Hela-S3	cervix:	n/a
49	chr4:9534388-9534438	PFSK-1	brain:	n/a
50	chr4:9558077-9558127	GM12892	blood:	n/a

(count:4 , 50 per page) page: 1

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

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

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

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

No data

Variant related genes	Relation type
ENSG00000249799	TF binding region
MIR548I2	TF binding region
ENSG00000249443	TF binding region
OR7E83P	TF binding region
ENSG00000244004	TF binding region
ENPP7P11	TF binding region
ENSG00000265901	TF binding region
ENSG00000242034	TF binding region
ENSG00000249799	CpG island
MIR548I2	CpG island
ENSG00000249443	CpG island
OR7E83P	CpG island
ENSG00000244004	CpG island
ENPP7P11	CpG island
ENSG00000265901	CpG island
ENSG00000242034	CpG island

Extended variants
information (count: 10844 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:10844 , 50 per page) page: 1 2 3 4 5 6 7 ... 217

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536944278	chr4:9496283-9496284	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs75363200	chr4:9496293-9496294	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs548929310	chr4:9496298-9496299	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs78199215	chr4:9496303-9496304	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569654310	chr4:9496304-9496305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185499878	chr4:9496307-9496308	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553255015	chr4:9496311-9496312	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs148246352	chr4:9496314-9496315	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs576819493	chr4:9496319-9496320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4974887	chr4:9496343-9496344	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs368640614	chr4:9496347-9496348	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542036092	chr4:9496357-9496358	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs78113550	chr4:9496371-9496372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs386671486	chr4:9496389-9496390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs146525859	chr4:9496391-9496392	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs188300165	chr4:9496426-9496427	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs116426371	chr4:9496460-9496461	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565291141	chr4:9496461-9496462	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181800228	chr4:9496470-9496471	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561466664	chr4:9496477-9496478	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115875634	chr4:9496490-9496491	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559671214	chr4:9496492-9496493	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186506008	chr4:9496497-9496498	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548817750	chr4:9496502-9496503	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2049543	chr4:9496515-9496516	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs191746345	chr4:9496517-9496518	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367591137	chr4:9496535-9496536	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183572039	chr4:9496554-9496555	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs10019949	chr4:9496569-9496570	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs186481399	chr4:9496584-9496585	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs199563513	chr4:9496587-9496588	ZNF genes & repeats Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10017204	chr4:9496607-9496608	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs567829759	chr4:9496613-9496614	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs535243356	chr4:9496623-9496624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs139110070	chr4:9496638-9496639	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs55748497	chr4:9496656-9496657	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs372127987	chr4:9496661-9496662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs558678671	chr4:9496664-9496665	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs182528210	chr4:9496674-9496675	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs386671487	chr4:9496682-9496683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs559765379	chr4:9496683-9496684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191353331	chr4:9496684-9496685	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs183153243	chr4:9496691-9496692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs10006179	chr4:9496692-9496693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs376715651	chr4:9496695-9496696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs55706196	chr4:9496699-9496700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs74496625	chr4:9496701-9496702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs532332262	chr4:9496721-9496722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552859642	chr4:9496728-9496729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs570334782	chr4:9496729-9496730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	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
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:922 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9484800-9503800	Weak transcription	Right Atrium	heart
2	chr4:9495800-9496800	Enhancers	Fetal Thymus	thymus
3	chr4:9496200-9496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr4:9496200-9496800	Enhancers	Thymus	Thymus
5	chr4:9496200-9497000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr4:9496400-9496600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:9496400-9496800	Enhancers	Primary hematopoietic stem cells	blood
8	chr4:9496600-9499000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:9496800-9499600	Weak transcription	Primary hematopoietic stem cells	blood
10	chr4:9499000-9499200	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
11	chr4:9499000-9499200	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
12	chr4:9499000-9499600	Enhancers	Liver	Liver
13	chr4:9499000-9500400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
14	chr4:9499000-9500600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:9499200-9499400	Bivalent Enhancer	Fetal Thymus	thymus
16	chr4:9499200-9499600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr4:9499200-9499800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr4:9499200-9499800	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
19	chr4:9499200-9500200	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
20	chr4:9499200-9500200	Bivalent Enhancer	Adipose Nuclei	Adipose
21	chr4:9499200-9500400	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
22	chr4:9499200-9500400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr4:9499200-9500600	Active TSS	H9 Cell Line	embryonic stem cell
24	chr4:9499200-9500600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
25	chr4:9499200-9500600	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
26	chr4:9499200-9500600	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
27	chr4:9499200-9500600	Active TSS	Breast Myoepithelial Primary Cells	Breast
28	chr4:9499400-9499600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr4:9499400-9499600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr4:9499400-9499600	Active TSS	Brain Germinal Matrix	brain
31	chr4:9499400-9499600	Enhancers	Colonic Mucosa	Colon
32	chr4:9499400-9499600	Active TSS	Fetal Brain Female	brain
33	chr4:9499400-9499800	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:9499400-9499800	Enhancers	Lung	lung
35	chr4:9499400-9500200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:9499400-9500400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
37	chr4:9499400-9500400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
38	chr4:9499400-9500600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
39	chr4:9499600-9499800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr4:9499600-9499800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr4:9499600-9499800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:9499600-9499800	Bivalent/Poised TSS	Fetal Intestine Large	intestine
43	chr4:9499600-9499800	Bivalent Enhancer	Fetal Lung	lung
44	chr4:9499600-9500000	Active TSS	Primary T cells from cord blood	blood
45	chr4:9499600-9500000	Enhancers	Sigmoid Colon	Sigmoid Colon
46	chr4:9499600-9500200	Bivalent/Poised TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:9499600-9500200	Bivalent/Poised TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:9499600-9500200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr4:9499600-9500200	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
50	chr4:9499600-9500200	Bivalent Enhancer	Brain Hippocampus Middle	brain

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