Variant report

Variant	esv2761619
Chromosome Location	chr10:97719520-97746180
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	chr10:97734790-97734844	HepG2	liver:	n/a	n/a
2	ATF1	chr10:97723333-97723782	K562	blood:	n/a	n/a
3	CEBPB	chr10:97739495-97739715	HepG2	liver:	n/a	chr10:97739592-97739603
4	CEBPB	chr10:97739558-97739704	A549	lung:	n/a	chr10:97739592-97739603
5	CEBPB	chr10:97736079-97736281	HepG2	liver:	n/a	chr10:97736090-97736098
6	CEBPB	chr10:97724480-97724763	A549	lung:	n/a	chr10:97724621-97724632
7	CEBPB	chr10:97724480-97724698	K562	blood:	n/a	chr10:97724621-97724632
8	CEBPB	chr10:97724477-97724677	HepG2	liver:	n/a	chr10:97724621-97724632
9	CEBPB	chr10:97724513-97724780	IMR90	lung:	n/a	chr10:97724621-97724632
10	CEBPB	chr10:97736057-97736668	HepG2	liver:	n/a	chr10:97736090-97736098
11	CTCF	chr10:97730560-97730710	GM12868	blood:	n/a	n/a
12	CTCF	chr10:97741038-97741115	MCF-7	breast:	n/a	n/a
13	CTCF	chr10:97721176-97721229	GM13977	blood:	n/a	n/a
14	ELF1	chr10:97736070-97736353	HepG2	liver:	n/a	chr10:97736259-97736270
15	FOXA1	chr10:97736030-97736431	HepG2	liver:	n/a	n/a
16	FOXA1	chr10:97736961-97737292	HepG2	liver:	n/a	chr10:97737156-97737168 chr10:97737160-97737172
17	GATA3	chr10:97722942-97723131	SH-SY5Y	brain:	n/a	n/a
18	GATA3	chr10:97722932-97723502	MCF-7	breast:	n/a	n/a
19	GATA3	chr10:97722823-97723406	MCF-7	breast:	n/a	chr10:97722834-97722841
20	HNF4A	chr10:97735993-97736331	HepG2	liver:	n/a	chr10:97736225-97736233 chr10:97736219-97736234 chr10:97736227-97736235 chr10:97736218-97736233
21	JUN	chr10:97735396-97735712	HepG2	liver:	n/a	chr10:97735520-97735529 chr10:97735522-97735535
22	JUND	chr10:97735355-97735672	HepG2	liver:	n/a	chr10:97735520-97735529
23	MAFK	chr10:97734237-97734284	HepG2	liver:	n/a	n/a
24	MAFK	chr10:97730557-97730582	H1-hESC	embryonic stem cell:	n/a	n/a
25	MYC	chr10:97740975-97741119	MCF-7	breast:	n/a	n/a
26	MYC	chr10:97741083-97741119	MCF-7	breast:	n/a	n/a
27	MYC	chr10:97742094-97742466	A549	lung:	n/a	n/a
28	MYC	chr10:97723478-97723549	MCF10A-Er-Src	breast:	n/a	n/a
29	POLR2A	chr10:97740921-97741120	MCF-7	breast:	n/a	n/a
30	POLR2A	chr10:97734650-97734743	GM12878	blood:	n/a	n/a
31	POLR2A	chr10:97723543-97723702	GM12891	blood:	n/a	n/a
32	POLR2A	chr10:97724092-97724254	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr10:97728917-97728922	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr10:97740967-97741161	MCF-7	breast:	n/a	n/a
35	POLR2A	chr10:97740953-97740957	MCF-7	breast:	n/a	n/a
36	RAD21	chr10:97730633-97730675	A549	lung:	n/a	n/a
37	RUNX3	chr10:97723332-97723721	GM12878	blood:	n/a	n/a
38	SIN3AK20	chr10:97722827-97723573	MCF-7	breast:	n/a	n/a
39	SP1	chr10:97736099-97736381	HepG2	liver:	n/a	n/a
40	SPI1	chr10:97724652-97724889	GM12891	blood:	n/a	n/a
41	SPI1	chr10:97724718-97724859	GM12878	blood:	n/a	n/a
42	SPI1	chr10:97734497-97734756	GM12891	blood:	n/a	chr10:97734505-97734514
43	SPI1	chr10:97736248-97736482	GM12878	blood:	n/a	chr10:97736259-97736272 chr10:97736258-97736271 chr10:97736262-97736269
44	SPI1	chr10:97738979-97739208	GM12891	blood:	n/a	chr10:97739130-97739143 chr10:97739132-97739141
45	SPI1	chr10:97724678-97724906	GM12891	blood:	n/a	n/a
46	SPI1	chr10:97738984-97739222	GM12891	blood:	n/a	chr10:97739130-97739143 chr10:97739132-97739141
47	SPI1	chr10:97724556-97724924	HL-60	blood:	n/a	n/a
48	SPI1	chr10:97738939-97739340	HL-60	blood:	n/a	chr10:97739130-97739143 chr10:97739132-97739141
49	SPI1	chr10:97738966-97739221	GM12878	blood:	n/a	chr10:97739130-97739143 chr10:97739132-97739141
50	SPI1	chr10:97736254-97736527	GM12891	blood:	n/a	chr10:97736259-97736272 chr10:97736258-97736271 chr10:97736262-97736269

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr10:97732990-97733040	SKMC	muscle:	n/a
2	chr10:97732990-97733040	NH-A	brain:	n/a
3	chr10:97732990-97733040	NHBE	bronchial:	n/a
4	chr10:97732990-97733040	AG09309	skin:	n/a
5	chr10:97732990-97733040	AG10803	skin:	n/a
6	chr10:97732990-97733040	BJ	skin:	n/a
7	chr10:97732990-97733040	MCF10A-Er-Src	breast:	n/a
8	chr10:97732990-97733040	ECC-1	luminal epithelium:	n/a
9	chr10:97732488-97732538	K562	blood:	n/a
10	chr10:97732488-97732538	BJ	skin:	n/a
11	chr10:97732488-97732538	SAEC	small airway:	n/a
12	chr10:97732990-97733040	HMEC	breast:	n/a
13	chr10:97732488-97732538	ovcar-3	ovarian:	n/a
14	chr10:97732488-97732538	RPTEC	kidney:	n/a
15	chr10:97732990-97733040	SK-N-SH_RA	brain:	n/a
16	chr10:97732990-97733040	PFSK-1	brain:	n/a
17	chr10:97732488-97732538	GM12891	blood:	n/a
18	chr10:97732488-97732538	AG09319	gingival:	n/a
19	chr10:97732488-97732538	HUVEC	blood vessel:	n/a
20	chr10:97732990-97733040	HEEpiC	esophagus:	n/a
21	chr10:97732488-97732538	U87	brain:	n/a
22	chr10:97732990-97733040	ovcar-3	ovarian:	n/a
23	chr10:97732488-97732538	HL-60	blood:	n/a
24	chr10:97732990-97733040	PrEC	prostate:	n/a
25	chr10:97732488-97732538	AG04449	skin:	fetal
26	chr10:97732990-97733040	HIPEpiC	eye:	n/a
27	chr10:97732488-97732538	GM12892	blood:	n/a
28	chr10:97732488-97732538	MCF-7	breast:	n/a
29	chr10:97732488-97732538	HEEpiC	esophagus:	n/a
30	chr10:97732488-97732538	NHDF-neo	bronchial:	n/a
31	chr10:97732990-97733040	NB4	blood:	n/a
32	chr10:97732488-97732538	PANC-1	pancreas:	n/a
33	chr10:97732990-97733040	SK-N-SH	brain:	n/a
34	chr10:97732990-97733040	GM12892	blood:	n/a
35	chr10:97732990-97733040	H1-hESC	embryonic stem cell:	embryo
36	chr10:97732990-97733040	NHDF-neo	bronchial:	n/a
37	chr10:97732488-97732538	NB4	blood:	n/a
38	chr10:97732488-97732538	SK-N-SH	brain:	n/a
39	chr10:97732990-97733040	Jurkat	blood:	n/a
40	chr10:97732990-97733040	HRPEpiC	eye:	n/a
41	chr10:97732488-97732538	IMR90	lung:	fetal
42	chr10:97732488-97732538	HCPEpiC	choroid plexus:	n/a
43	chr10:97732990-97733040	MCF-7	breast:	n/a
44	chr10:97732990-97733040	HCM	heart:	n/a
45	chr10:97732488-97732538	SK-N-MC	brain:	n/a
46	chr10:97732488-97732538	HepG2	liver:	n/a
47	chr10:97732488-97732538	ProgFib	skin:	n/a
48	chr10:97732990-97733040	AoSMC	blood vessel:	n/a
49	chr10:97732488-97732538	HMEC	breast:	n/a
50	chr10:97732488-97732538	HAEpiC	amniotic membrane:	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:97746122..97748818-chr10:97753342..97755007,2	K562	blood:
2	chr10:97715075..97717525-chr10:97719176..97721345,2	K562	blood:
3	chr10:97730369..97732465-chr10:97746153..97748882,2	K562	blood:
4	chr10:97730369..97732465-chr10:97746153..97748882,2	K562	blood:
5	chr10:97733135..97735201-chr10:97739449..97742171,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CCNJ-7	chr10:97721331-97721726	NONHSAT015783
2	lnc-CCNJ-7	chr10:97725653-97725710	NONHSAT015783

Variant related genes	Relation type
CC2D2B	TF binding region
ENSG00000269920	TF binding region
ENSG00000269948	TF binding region
CC2D2B	CpG island
ENSG00000269920	CpG island
ENSG00000269948	CpG island
ENSG00000269920	chromatin interactions
ENSG00000269948	chromatin interactions

Extended variants
information (count: 669 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7909124	chr10:97719520-97719521	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs559301751	chr10:97719671-97719672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs142000546	chr10:97719704-97719705	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs113667292	chr10:97719794-97719795	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548047817	chr10:97719826-97719827	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs551339245	chr10:97719922-97719923	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573589967	chr10:97719938-97719939	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs146330748	chr10:97719948-97719949	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs530686936	chr10:97720068-97720069	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs187978907	chr10:97720154-97720155	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs192249710	chr10:97720192-97720193	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs182824438	chr10:97720241-97720242	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs78180309	chr10:97720258-97720259	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs76786281	chr10:97720259-97720260	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs5787166	chr10:97720279-97720280	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs398097161	chr10:97720287-97720288	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs528363070	chr10:97720332-97720333	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs118118621	chr10:97720404-97720405	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs1336458	chr10:97720429-97720430	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs10219061	chr10:97720451-97720452	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs187859477	chr10:97720531-97720532	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs535352984	chr10:97720556-97720557	ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs555261135	chr10:97720649-97720650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563621203	chr10:97720715-97720716	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs575089167	chr10:97720719-97720720	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs550038321	chr10:97720738-97720739	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs557261902	chr10:97720744-97720745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs78640251	chr10:97720749-97720750	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs149504762	chr10:97720824-97720825	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559337819	chr10:97720850-97720851	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs376709854	chr10:97720855-97720856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs541726572	chr10:97720884-97720885	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs570110119	chr10:97720909-97720910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530706874	chr10:97720914-97720915	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs550788404	chr10:97720920-97720921	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs371795073	chr10:97720994-97720995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs148681668	chr10:97720998-97720999	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs537314122	chr10:97721013-97721014	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs535525311	chr10:97721023-97721024	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192586616	chr10:97721031-97721032	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs142063011	chr10:97721034-97721035	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185417927	chr10:97721064-97721065	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs566482037	chr10:97721065-97721066	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs377480358	chr10:97721111-97721112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs535392283	chr10:97721115-97721116	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs555398403	chr10:97721133-97721134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs111331742	chr10:97721208-97721209	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs537323297	chr10:97721213-97721214	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs557554270	chr10:97721220-97721221	Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs577333225	chr10:97721239-97721240	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Melanoma	18172304	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Ewing''s sarcoma	17952124	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	20724749	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Cockayne syndrome	18421352	CNVD
Glioblastoma	16823260	CNVD
Medulloblastoma	16968546	CNVD
Neuroblastoma	17533364	CNVD
Squamous cell cancer	21044232	CNVD
Glioma	21971842	CNVD
Cancer	21637783	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Lung cancer	18438408	CNVD
Usher syndrome	20538994	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	20729466	CNVD
Paraganglioma	17535989	CNVD
Submicroscopic aberration syndrome	21292638	CNVD
Prostate cancer	16573809	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Pulmonary chondroma	17535989	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	22032731	CNVD
Ovarian cancer	20844748	CNVD
Glioblastoma multiforme	17002787	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cervical cancer	21062161	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	24453001	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16912164	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97720200-97720600	ZNF genes & repeats	Aorta	Aorta
2	chr10:97720600-97722600	Weak transcription	Aorta	Aorta
3	chr10:97720800-97731400	Weak transcription	Left Ventricle	heart
4	chr10:97722200-97723200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:97722400-97723000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
6	chr10:97722600-97722800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr10:97722600-97722800	ZNF genes & repeats	Aorta	Aorta
8	chr10:97722600-97723200	Enhancers	Primary T helper cells PMA-I stimulated	--
9	chr10:97722600-97723200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr10:97722600-97723800	Enhancers	Primary hematopoietic stem cells	blood
11	chr10:97722600-97725400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr10:97722800-97723400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr10:97722800-97724600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr10:97722800-97725000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
15	chr10:97722800-97725000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr10:97722800-97729200	Weak transcription	Aorta	Aorta
17	chr10:97723000-97723200	Enhancers	Primary T helper naive cells from peripheral blood	blood
18	chr10:97723000-97723200	Enhancers	GM12878-XiMat	blood
19	chr10:97723000-97723200	Enhancers	K562	blood
20	chr10:97723000-97723400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr10:97723000-97723600	Enhancers	Primary T cells from cord blood	blood
22	chr10:97723000-97724000	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr10:97723000-97724800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr10:97723000-97725400	Enhancers	Primary B cells from peripheral blood	blood
25	chr10:97723200-97723600	Enhancers	Primary B cells from cord blood	blood
26	chr10:97723200-97723600	Enhancers	Primary T cells fromperipheralblood	blood
27	chr10:97723200-97723600	Flanking Active TSS	K562	blood
28	chr10:97723200-97723800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr10:97723200-97724000	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr10:97723200-97724000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
31	chr10:97723200-97724000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr10:97723200-97724000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
33	chr10:97723200-97724000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr10:97723200-97724000	Flanking Active TSS	GM12878-XiMat	blood
35	chr10:97723200-97724200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chr10:97723200-97724800	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr10:97723400-97723800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
38	chr10:97723400-97723800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
39	chr10:97723400-97723800	Bivalent Enhancer	Dnd41	blood
40	chr10:97723400-97724000	Enhancers	Adipose Nuclei	Adipose
41	chr10:97723600-97723800	Enhancers	K562	blood
42	chr10:97723600-97724000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr10:97723600-97724000	Flanking Active TSS	Primary T cells from cord blood	blood
44	chr10:97723600-97724000	Active TSS	Primary T cells fromperipheralblood	blood
45	chr10:97723600-97724400	Flanking Active TSS	Primary B cells from cord blood	blood
46	chr10:97723800-97724000	Flanking Active TSS	Primary hematopoietic stem cells	blood
47	chr10:97723800-97724800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr10:97723800-97724800	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr10:97724000-97724600	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr10:97724000-97724600	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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