Variant report

Variant	esv10713
Chromosome Location	chr4:10136109-10153485
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	ATF2	chr4:10152775-10153075	GM12878	blood:	n/a	n/a
2	BHLHE40	chr4:10142964-10143314	K562	blood:	n/a	n/a
3	CHD2	chr4:10142301-10142459	HepG2	liver:	n/a	n/a
4	CHD2	chr4:10143239-10143269	K562	blood:	n/a	n/a
5	CTCF	chr4:10143000-10143150	A549	lung:	n/a	n/a
6	CTCF	chr4:10143140-10143290	GM12872	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
7	CTCF	chr4:10143120-10143270	HMEC	breast:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
8	CTCF	chr4:10142620-10142770	HRPEpiC	eye:	n/a	n/a
9	CTCF	chr4:10146200-10146350	HEK293	kidney:	n/a	n/a
10	CTCF	chr4:10143160-10143310	BE2_C	brain:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
11	CTCF	chr4:10143100-10143250	HCM	heart:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
12	CTCF	chr4:10143100-10143250	HCFaa	heart:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
13	CTCF	chr4:10142737-10143429	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
14	CTCF	chr4:10143120-10143270	GM12872	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
15	CTCF	chr4:10142700-10142850	BJ	skin:	n/a	n/a
16	CTCF	chr4:10143140-10143290	HRPEpiC	eye:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
17	CTCF	chr4:10142900-10143050	GM12864	blood:	n/a	chr4:10142953-10142962
18	CTCF	chr4:10146260-10146410	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr4:10143060-10143210	GM12871	blood:	n/a	n/a
20	CTCF	chr4:10143186-10143191	GM10266	blood:	n/a	n/a
21	CTCF	chr4:10143140-10143290	WERI-Rb-1	eye:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
22	CTCF	chr4:10142633-10142773	K562	blood:	n/a	n/a
23	CTCF	chr4:10142815-10143400	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
24	CTCF	chr4:10143200-10143350	HRPEpiC	eye:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
25	CTCF	chr4:10143180-10143330	SAEC	small airway:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
26	CTCF	chr4:10143193-10143253	GM10266	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
27	CTCF	chr4:10146160-10146310	GM12864	blood:	n/a	n/a
28	CTCF	chr4:10143140-10143290	NB4	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
29	CTCF	chr4:10143120-10143270	HRE	kidney:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
30	CTCF	chr4:10143180-10143330	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
31	CTCF	chr4:10142808-10143435	K562	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
32	CTCF	chr4:10143160-10143310	GM12872	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
33	CTCF	chr4:10146180-10146330	GM12864	blood:	n/a	n/a
34	CTCF	chr4:10142560-10142710	SAEC	small airway:	n/a	n/a
35	CTCF	chr4:10142640-10142790	HepG2	liver:	n/a	n/a
36	CTCF	chr4:10146180-10146330	K562	blood:	n/a	n/a
37	CTCF	chr4:10142560-10143448	H1-hESC	embryonic stem cell:	n/a	chr4:10143232-10143241 chr4:10143229-10143247 chr4:10142953-10142962
38	CTCF	chr4:10143220-10143370	BE2_C	brain:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
39	CTCF	chr4:10143184-10143283	GM12892	blood:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
40	CTCF	chr4:10142600-10142750	K562	blood:	n/a	n/a
41	CTCF	chr4:10143209-10143215	NHEK	skin:	n/a	n/a
42	CTCF	chr4:10142640-10142790	HEK293	kidney:	n/a	n/a
43	CTCF	chr4:10146240-10146390	GM12875	blood:	n/a	n/a
44	CTCF	chr4:10143120-10143270	Caco-2	colon:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
45	CTCF	chr4:10142587-10142788	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr4:10143120-10143270	HCT-116	colon:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
47	CTCF	chr4:10142873-10143086	H1-hESC	embryonic stem cell:	n/a	chr4:10142953-10142962
48	CTCF	chr4:10143120-10143270	HBMEC	blood vessel:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
49	CTCF	chr4:10143180-10143330	HEK293	kidney:	n/a	chr4:10143232-10143241 chr4:10143229-10143247
50	CTCF	chr4:10143120-10143270	Hela-S3	cervix:	n/a	chr4:10143232-10143241 chr4:10143229-10143247

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:10147330-10147380	HCPEpiC	choroid plexus:	n/a
2	chr4:10147302-10147352	HRE	kidney:	n/a
3	chr4:10147330-10147380	HCPEpiC	choroid plexus:	n/a
4	chr4:10147302-10147352	HRE	kidney:	n/a
5	chr4:10143053-10143103	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:10147100-10147150	A549	lung:	n/a
7	chr4:10147302-10147352	HepG2	liver:	n/a
8	chr4:10147330-10147380	ProgFib	skin:	n/a
9	chr4:10143053-10143103	NT2-D1	testis:	n/a
10	chr4:10145483-10145533	GM12892	blood:	n/a
11	chr4:10147302-10147352	SKMC	muscle:	n/a
12	chr4:10145483-10145533	HEK293	kidney:	embryo
13	chr4:10147606-10147656	K562	blood:	n/a
14	chr4:10147606-10147656	HCT-116	colon:	n/a
15	chr4:10145483-10145533	AoSMC	blood vessel:	n/a
16	chr4:10147330-10147380	GM19239	blood:	n/a
17	chr4:10147302-10147352	HRPEpiC	eye:	n/a
18	chr4:10149849-10149899	AG10803	skin:	n/a
19	chr4:10149849-10149899	HMEC	breast:	n/a
20	chr4:10149849-10149899	HRPEpiC	eye:	n/a
21	chr4:10147302-10147352	HCPEpiC	choroid plexus:	n/a
22	chr4:10147606-10147656	H1-hESC	embryonic stem cell:	embryo
23	chr4:10149849-10149899	SAEC	small airway:	n/a
24	chr4:10147606-10147656	SK-N-SH	brain:	n/a
25	chr4:10147100-10147150	SK-N-MC	brain:	n/a
26	chr4:10149849-10149899	Jurkat	blood:	n/a
27	chr4:10145483-10145533	SAEC	small airway:	n/a
28	chr4:10149849-10149899	GM19239	blood:	n/a
29	chr4:10143053-10143103	MCF10A-Er-Src	breast:	n/a
30	chr4:10149849-10149899	PFSK-1	brain:	n/a
31	chr4:10145483-10145533	Hela-S3	cervix:	n/a
32	chr4:10147606-10147656	HAEpiC	amniotic membrane:	n/a
33	chr4:10147330-10147380	SAEC	small airway:	n/a
34	chr4:10149849-10149899	AG09309	skin:	n/a
35	chr4:10143053-10143103	SAEC	small airway:	n/a
36	chr4:10147100-10147150	Hela-S3	cervix:	n/a
37	chr4:10147606-10147656	MCF-7	breast:	n/a
38	chr4:10147302-10147352	PANC-1	pancreas:	n/a
39	chr4:10143053-10143103	SKMC	muscle:	n/a
40	chr4:10143053-10143103	NHDF-neo	bronchial:	n/a
41	chr4:10145483-10145533	NH-A	brain:	n/a
42	chr4:10147330-10147380	SK-N-SH_RA	brain:	n/a
43	chr4:10147330-10147380	K562	blood:	n/a
44	chr4:10149849-10149899	H1-hESC	embryonic stem cell:	embryo
45	chr4:10147606-10147656	SAEC	small airway:	n/a
46	chr4:10147100-10147150	ECC-1	luminal epithelium:	n/a
47	chr4:10147302-10147352	MCF10A-Er-Src	breast:	n/a
48	chr4:10147330-10147380	ECC-1	luminal epithelium:	n/a
49	chr4:10145483-10145533	HPAEpiC	pulmonary alveolar:	n/a
50	chr4:10147038-10147088	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10151902..10153544-chr4:10159740..10162552,2	K562	blood:
2	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
3	chr4:10110208..10112839-chr4:10141638..10144449,2	MCF-7	breast:
4	chr4:10143164..10147494-chr4:10150670..10153852,4	K562	blood:
5	chr4:10140841..10143166-chr4:10164924..10167000,2	K562	blood:
6	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
7	chr4:10147647..10149912-chr4:10150747..10153139,2	K562	blood:
8	chr4:10117694..10121179-chr4:10148695..10151564,3	MCF-7	breast:
9	chr4:10117542..10119864-chr4:10151862..10154716,2	MCF-7	breast:
10	chr4:10137029..10138548-chr4:10444331..10446997,2	K562	blood:
11	chr4:10150688..10152239-chr4:10154005..10156791,2	K562	blood:
12	chr4:10146309..10149123-chr4:10156130..10158993,2	K562	blood:
13	chr4:10147623..10149514-chr4:10156130..10157999,2	K562	blood:
14	chr4:10118040..10120090-chr4:10149414..10151081,2	K562	blood:
15	chr4:10117985..10121218-chr4:10149186..10152668,4	MCF-7	breast:
16	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
17	chr4:10117300..10124855-chr4:10138380..10145377,13	MCF-7	breast:
18	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
19	chr4:10138009..10140287-chr4:10142395..10145088,2	MCF-7	breast:
20	chr4:10142152..10144542-chr4:10456013..10458159,2	K562	blood:
21	chr4:10140012..10142690-chr4:10152544..10154199,2	K562	blood:
22	chr4:10141623..10144820-chr4:10145857..10148531,3	K562	blood:
23	chr4:10124769..10127534-chr4:10135159..10136966,2	MCF-7	breast:
24	chr4:10137227..10139603-chr4:10183343..10185587,3	K562	blood:
25	chr4:10142468..10145387-chr4:10146611..10148310,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-4	chr4:10151989-10152058	NONHSAT095472
2	lnc-WDR1-2	chr4:10144991-10145279	NONHSAT095429

Variant related genes	Relation type
ENSG00000250393	TF binding region
ENSG00000250393	CpG island
ENSG00000071127	chromatin interactions
ENSG00000223086	chromatin interactions
ENSG00000250393	chromatin interactions

Extended variants
information (count: 1513 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:1513 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546532515	chr4:10136804-10136805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs4358401	chr4:10136807-10136808	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534075866	chr4:10136809-10136810	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs192815279	chr4:10136831-10136832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs555738499	chr4:10136834-10136835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs200497290	chr4:10136842-10136843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs201678649	chr4:10136843-10136844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs535241108	chr4:10136857-10136858	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs544230548	chr4:10136874-10136875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184378068	chr4:10136876-10136877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs189330687	chr4:10136883-10136884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376714982	chr4:10136893-10136894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58198247	chr4:10136895-10136896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs397941722	chr4:10136897-10136898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs138501326	chr4:10136903-10136904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558951628	chr4:10136911-10136912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556593178	chr4:10136933-10136934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115885584	chr4:10136960-10136961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs535346697	chr4:10136964-10136965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs189419756	chr4:10136978-10136979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs193124692	chr4:10136981-10136982	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs184806940	chr4:10136983-10136984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs575455464	chr4:10136987-10136988	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs56201573	chr4:10137018-10137019	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs76547354	chr4:10137029-10137030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs529995742	chr4:10137032-10137033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs545872462	chr4:10137034-10137035	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs564109921	chr4:10137040-10137041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs189271355	chr4:10137041-10137042	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181679869	chr4:10137043-10137044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546891436	chr4:10137047-10137048	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs556261124	chr4:10137050-10137051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs529130275	chr4:10137062-10137063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs550409124	chr4:10137090-10137091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138645884	chr4:10137093-10137094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185859750	chr4:10137096-10137097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs873984	chr4:10137125-10137126	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs71603990	chr4:10137129-10137130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552359526	chr4:10137133-10137134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs189583960	chr4:10137161-10137162	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs564700457	chr4:10137181-10137182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs534742095	chr4:10137185-10137186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10008628	chr4:10137201-10137202	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552747993	chr4:10137202-10137203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs118181336	chr4:10137229-10137230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181125921	chr4:10137232-10137233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs142740833	chr4:10137245-10137246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs186039170	chr4:10137273-10137274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs146071624	chr4:10137294-10137295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191139076	chr4:10137295-10137296	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
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
Wilms tumour	21544195	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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10136800-10137400	Enhancers	NHEK	skin
2	chr4:10136800-10137800	Enhancers	Fetal Heart	heart
3	chr4:10142400-10142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr4:10142600-10142800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr4:10142600-10143000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:10142600-10143200	Enhancers	Fetal Thymus	thymus
7	chr4:10142800-10143000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
8	chr4:10142800-10143200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr4:10142800-10143200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:10142800-10143200	Enhancers	H9 Cell Line	embryonic stem cell
11	chr4:10142800-10143200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:10142800-10143200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
13	chr4:10142800-10151800	Weak transcription	Spleen	Spleen
14	chr4:10143000-10143200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr4:10143000-10143200	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr4:10143000-10143200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr4:10143000-10143200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:10143200-10143600	Enhancers	Rectal Mucosa Donor 29	rectum
19	chr4:10143200-10149800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr4:10146200-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr4:10146400-10146800	Enhancers	Monocytes-CD14+_RO01746	blood
22	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr4:10146400-10147000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:10146400-10147600	Enhancers	Primary B cells from peripheral blood	blood
25	chr4:10146600-10147200	Bivalent Enhancer	Primary B cells from cord blood	blood
26	chr4:10149800-10150000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:10151000-10151200	Enhancers	Fetal Stomach	stomach
28	chr4:10151200-10164400	Weak transcription	Right Atrium	heart
29	chr4:10151400-10152400	Weak transcription	Fetal Stomach	stomach
30	chr4:10151800-10152000	Enhancers	Spleen	Spleen
31	chr4:10151800-10153000	Enhancers	Fetal Muscle Leg	muscle
32	chr4:10152000-10152200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
33	chr4:10152000-10153600	Enhancers	Primary B cells from cord blood	blood
34	chr4:10152200-10153800	Enhancers	Primary B cells from peripheral blood	blood
35	chr4:10152400-10152800	Enhancers	Fetal Stomach	stomach
36	chr4:10152600-10152800	Flanking Active TSS	GM12878-XiMat	blood
37	chr4:10152800-10153400	Enhancers	GM12878-XiMat	blood

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