Variant report

Variant	nsv878693
Chromosome Location	chr4:10263245-10286301
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	BACH1	chr4:10277398-10277423	K562	blood:	n/a	n/a
2	CEBPB	chr4:10267288-10267523	A549	lung:	n/a	chr4:10267446-10267457
3	CEBPB	chr4:10267329-10267510	HepG2	liver:	n/a	chr4:10267446-10267457
4	CTCF	chr4:10267520-10267670	NHEK	skin:	n/a	chr4:10267591-10267599
5	CTCF	chr4:10282060-10282210	GM12872	blood:	n/a	chr4:10282153-10282162
6	CTCF	chr4:10273284-10273382	K562	blood:	n/a	n/a
7	CTCF	chr4:10266760-10266910	GM12867	blood:	n/a	n/a
8	CTCF	chr4:10282080-10282230	HEK293	kidney:	n/a	chr4:10282153-10282162
9	CTCF	chr4:10273213-10273430	K562	blood:	n/a	n/a
10	CTCF	chr4:10282040-10282190	WERI-Rb-1	eye:	n/a	chr4:10282153-10282162
11	CTCF	chr4:10282100-10282250	K562	blood:	n/a	chr4:10282153-10282162
12	CTCF	chr4:10282100-10282250	SAEC	small airway:	n/a	chr4:10282153-10282162
13	CTCF	chr4:10282080-10282230	SAEC	small airway:	n/a	chr4:10282153-10282162
14	E2F4	chr4:10273012-10273166	MCF10A-Er-Src	breast:	n/a	n/a
15	E2F4	chr4:10274558-10275032	MCF10A-Er-Src	breast:	n/a	n/a
16	FOS	chr4:10280945-10281198	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr4:10283809-10284009	MCF10A-Er-Src	breast:	n/a	chr4:10283889-10283899 chr4:10283842-10283852 chr4:10283843-10283851
18	FOS	chr4:10285423-10285752	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr4:10283686-10284014	MCF10A-Er-Src	breast:	n/a	chr4:10283889-10283899 chr4:10283842-10283852 chr4:10283843-10283851
20	FOS	chr4:10285330-10285916	MCF10A-Er-Src	breast:	n/a	chr4:10285371-10285382
21	FOS	chr4:10280783-10281240	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr4:10274597-10275143	MCF10A-Er-Src	breast:	n/a	chr4:10274960-10274970 chr4:10274961-10274969 chr4:10274960-10274970
23	FOS	chr4:10285372-10285786	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr4:10283667-10284014	MCF10A-Er-Src	breast:	n/a	chr4:10283889-10283899 chr4:10283842-10283852 chr4:10283843-10283851
25	FOS	chr4:10283745-10283975	MCF10A-Er-Src	breast:	n/a	chr4:10283889-10283899 chr4:10283842-10283852 chr4:10283843-10283851
26	FOS	chr4:10274631-10275073	MCF10A-Er-Src	breast:	n/a	chr4:10274960-10274970 chr4:10274961-10274969 chr4:10274960-10274970
27	FOS	chr4:10274596-10275143	MCF10A-Er-Src	breast:	n/a	chr4:10274960-10274970 chr4:10274961-10274969 chr4:10274960-10274970
28	FOS	chr4:10281029-10281177	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr4:10277560-10277605	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr4:10285309-10285856	MCF10A-Er-Src	breast:	n/a	chr4:10285371-10285382
31	FOS	chr4:10277435-10277540	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr4:10268776-10268932	MCF10A-Er-Src	breast:	n/a	chr4:10268877-10268887 chr4:10268876-10268888 chr4:10268878-10268886 chr4:10268878-10268885 chr4:10268877-10268886
33	FOS	chr4:10274606-10275143	MCF10A-Er-Src	breast:	n/a	chr4:10274960-10274970 chr4:10274961-10274969 chr4:10274960-10274970
34	FOS	chr4:10268815-10268981	MCF10A-Er-Src	breast:	n/a	chr4:10268877-10268887 chr4:10268876-10268888 chr4:10268878-10268886 chr4:10268878-10268885 chr4:10268877-10268886
35	FOS	chr4:10268727-10268914	MCF10A-Er-Src	breast:	n/a	chr4:10268877-10268887 chr4:10268876-10268888 chr4:10268878-10268886 chr4:10268878-10268885 chr4:10268877-10268886
36	FOS	chr4:10277896-10278128	MCF10A-Er-Src	breast:	n/a	n/a
37	GATA1	chr4:10263970-10264666	PBDE	blood:	n/a	chr4:10264452-10264461
38	GATA2	chr4:10284702-10285125	HUVEC	blood vessel:	n/a	n/a
39	GTF2F1	chr4:10276577-10276647	H1-hESC	embryonic stem cell:	n/a	n/a
40	JUND	chr4:10277322-10278091	K562	blood:	n/a	n/a
41	MAFF	chr4:10275736-10275972	HepG2	liver:	n/a	chr4:10275860-10275878
42	MAFF	chr4:10264617-10264631	K562	blood:	n/a	n/a
43	MAFK	chr4:10275729-10276017	HepG2	liver:	n/a	chr4:10275861-10275876
44	MAFK	chr4:10275735-10275992	HepG2	liver:	n/a	chr4:10275861-10275876
45	MAFK	chr4:10286066-10286313	K562	blood:	n/a	n/a
46	MYC	chr4:10285110-10285880	MCF10A-Er-Src	breast:	n/a	chr4:10285333-10285342 chr4:10285413-10285423 chr4:10285412-10285421 chr4:10285412-10285422 chr4:10285411-10285424 chr4:10285413-10285422 chr4:10285412-10285423 chr4:10285413-10285422 chr4:10285411-10285426 chr4:10285411-10285424 chr4:10285411-10285424 chr4:10285412-10285423 chr4:10285413-10285423 chr4:10285413-10285422 chr4:10285412-10285422 chr4:10285411-10285424 chr4:10285412-10285423
47	MYC	chr4:10277464-10277494	MCF10A-Er-Src	breast:	n/a	n/a
48	MYC	chr4:10285276-10285729	MCF10A-Er-Src	breast:	n/a	chr4:10285333-10285342 chr4:10285413-10285423 chr4:10285412-10285421 chr4:10285412-10285422 chr4:10285411-10285424 chr4:10285413-10285422 chr4:10285412-10285423 chr4:10285413-10285422 chr4:10285411-10285426 chr4:10285411-10285424 chr4:10285411-10285424 chr4:10285412-10285423 chr4:10285413-10285423 chr4:10285413-10285422 chr4:10285412-10285422 chr4:10285411-10285424 chr4:10285412-10285423
49	MYC	chr4:10274631-10275351	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr4:10274623-10275000	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:10271663..10276718-chr4:10277557..10282432,8	K562	blood:
2	chr4:10262775..10265010-chr4:10265780..10268025,2	K562	blood:
3	chr4:10182494..10184635-chr4:10284696..10287291,2	K562	blood:
4	chr4:10255171..10260191-chr4:10262748..10268904,8	K562	blood:
5	chr4:10278587..10280479-chr4:10297418..10299087,2	K562	blood:
6	chr4:10274788..10276860-chr4:10285063..10286717,2	K562	blood:
7	chr4:10254361..10256671-chr4:10262474..10264248,2	K562	blood:
8	chr4:10271663..10276718-chr4:10277557..10282432,8	K562	blood:
9	chr4:10266281..10269337-chr4:10269908..10272870,3	K562	blood:
10	chr4:10262775..10265010-chr4:10265780..10268025,2	K562	blood:
11	chr4:10181799..10184639-chr4:10262185..10264664,2	K562	blood:
12	chr4:10271663..10274322-chr4:10278537..10280895,2	K562	blood:
13	chr4:10271663..10274322-chr4:10278537..10280895,2	K562	blood:
14	chr4:10207125..10208799-chr4:10284967..10286577,2	K562	blood:
15	chr4:10182494..10184107-chr4:10284696..10287149,2	K562	blood:
16	chr4:10257186..10261463-chr4:10263373..10268480,7	K562	blood:
17	chr4:10274788..10276860-chr4:10285063..10286717,2	K562	blood:
18	chr4:10266281..10269337-chr4:10269908..10272870,3	K562	blood:
19	chr4:10266886..10269236-chr4:10273082..10275523,2	K562	blood:
20	chr4:10266886..10269236-chr4:10273082..10275523,2	K562	blood:
21	chr4:10283364..10286619-chr4:10288507..10291288,3	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-WDR1-11	chr4:10269519-10269855	NONHSAT095492

Variant related genes	Relation type
ENSG00000250573	TF binding region
ENSG00000250040	TF binding region
ENSG00000250074	TF binding region
ENSG00000250040	chromatin interactions

Extended variants
information (count: 1582 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1582 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1541522	chr4:10263245-10263246	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs568498027	chr4:10263249-10263250	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs572597864	chr4:10263271-10263272	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559224156	chr4:10263283-10263284	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs543209155	chr4:10263284-10263285	Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs17406107	chr4:10263380-10263381	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs576102636	chr4:10263393-10263394	Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs76359787	chr4:10263414-10263415	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564909736	chr4:10263416-10263417	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs112582439	chr4:10263423-10263424	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs371545048	chr4:10263445-10263446	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs78104177	chr4:10263466-10263467	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs559692470	chr4:10263475-10263476	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs142618537	chr4:10263486-10263487	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs548383499	chr4:10263516-10263517	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs569725506	chr4:10263524-10263525	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs538362556	chr4:10263540-10263541	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549845645	chr4:10263566-10263567	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571345492	chr4:10263569-10263570	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs56292253	chr4:10263571-10263572	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553702398	chr4:10263594-10263595	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs572706877	chr4:10263624-10263625	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs553311893	chr4:10263650-10263651	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74511315	chr4:10263659-10263660	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555174762	chr4:10263680-10263681	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575003133	chr4:10263683-10263684	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543584638	chr4:10263716-10263717	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs564969751	chr4:10263725-10263726	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs567543901	chr4:10263757-10263758	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4697990	chr4:10263774-10263775	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs140875143	chr4:10263795-10263796	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs559359064	chr4:10263806-10263807	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs80143923	chr4:10263815-10263816	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs548164441	chr4:10263819-10263820	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs143958575	chr4:10263825-10263826	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563530706	chr4:10263835-10263836	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs530607305	chr4:10263838-10263839	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs369062462	chr4:10263887-10263888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs76690204	chr4:10263901-10263902	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs191655499	chr4:10263907-10263908	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs532429176	chr4:10263920-10263921	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146665339	chr4:10263989-10263990	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs565906712	chr4:10263999-10264000	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs140257514	chr4:10264013-10264014	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs546225133	chr4:10264015-10264016	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs564533289	chr4:10264046-10264047	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554955749	chr4:10264060-10264061	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs570277222	chr4:10264077-10264078	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs183014288	chr4:10264118-10264119	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs559156337	chr4:10264145-10264146	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

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
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:10262000-10263400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr4:10262000-10263400	Weak transcription	Fetal Thymus	thymus
3	chr4:10262000-10273800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:10262800-10263400	Weak transcription	Gastric	stomach
5	chr4:10262800-10264600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:10263000-10263400	Weak transcription	K562	blood
7	chr4:10263200-10263800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:10263400-10263600	Enhancers	Fetal Thymus	thymus
9	chr4:10263400-10263600	Enhancers	Gastric	stomach
10	chr4:10263400-10265600	Enhancers	K562	blood
11	chr4:10263600-10266800	Weak transcription	Fetal Thymus	thymus
12	chr4:10263600-10268200	Weak transcription	Gastric	stomach
13	chr4:10264600-10264800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr4:10264600-10264800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:10265600-10271000	Weak transcription	K562	blood
16	chr4:10266200-10266600	Enhancers	Thymus	Thymus
17	chr4:10266400-10266800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr4:10266800-10267000	Enhancers	Fetal Thymus	thymus
19	chr4:10267000-10273600	Weak transcription	Fetal Thymus	thymus
20	chr4:10267800-10268200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr4:10268200-10268800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:10268200-10269400	Enhancers	Gastric	stomach
23	chr4:10268400-10269200	Enhancers	NHEK	skin
24	chr4:10268400-10269400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr4:10268800-10269000	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr4:10268800-10273600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:10269000-10273800	Weak transcription	HMEC	breast
28	chr4:10269200-10269800	Enhancers	Duodenum Mucosa	Duodenum
29	chr4:10269200-10274600	Weak transcription	NHEK	skin
30	chr4:10269400-10274000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr4:10271000-10271800	Enhancers	K562	blood
32	chr4:10271400-10272200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr4:10271800-10277600	Weak transcription	K562	blood
34	chr4:10272200-10274000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:10273400-10274600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr4:10273600-10274400	Enhancers	Thymus	Thymus
37	chr4:10273600-10275200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:10273600-10275200	Enhancers	Fetal Thymus	thymus
39	chr4:10273800-10275000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr4:10273800-10275200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr4:10273800-10275400	Enhancers	HMEC	breast
42	chr4:10274000-10274400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr4:10274000-10274400	Enhancers	HSMM	muscle
44	chr4:10274000-10274600	Enhancers	HSMMtube	muscle
45	chr4:10274000-10274800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:10274000-10275200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr4:10274200-10274800	Enhancers	Osteobl	bone
48	chr4:10274400-10277600	Weak transcription	HSMM	muscle
49	chr4:10274600-10275200	Enhancers	NHEK	skin
50	chr4:10274600-10277200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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