Variant report

Variant	rs60964166
Chromosome Location	chr1:228463119-228463120
allele	C/G
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	TEAD4	chr1:228462845-228463184	K562	blood:	n/a	n/a
2	POLR2A	chr1:228463093-228464070	K562	blood:	n/a	n/a
3	CCNT2	chr1:228462955-228463732	K562	blood:	n/a	n/a
4	MAX	chr1:228463114-228464474	H1-hESC	embryonic stem cell:	n/a	chr1:228464133-228464140 chr1:228464032-228464041
5	RCOR1	chr1:228462777-228463320	K562	blood:	n/a	n/a
6	BHLHE40	chr1:228462908-228463176	K562	blood:	n/a	n/a
7	NRF1	chr1:228463112-228463334	H1-hESC	embryonic stem cell:	n/a	chr1:228463268-228463279
8	MAX	chr1:228462969-228464482	K562	blood:	n/a	chr1:228464133-228464140 chr1:228464032-228464041
9	E2F6	chr1:228462892-228463855	K562	blood:	n/a	chr1:228463368-228463378
10	ZNF263	chr1:228463050-228464329	K562	blood:	n/a	chr1:228463756-228463777 chr1:228463818-228463839
11	MXI1	chr1:228462959-228464346	IMR90	lung:	n/a	n/a
12	ELF1	chr1:228463118-228463999	K562	blood:	n/a	chr1:228463333-228463345
13	MYC	chr1:228462961-228463953	K562	blood:	n/a	n/a
14	UBTF	chr1:228462928-228463911	K562	blood:	n/a	n/a
15	MAX	chr1:228462751-228464565	K562	blood:	n/a	chr1:228464133-228464140 chr1:228464032-228464041
16	RCOR1	chr1:228462777-228463986	K562	blood:	n/a	n/a
17	GABPA	chr1:228462884-228463413	H1-hESC	embryonic stem cell:	n/a	n/a
18	MAX	chr1:228463059-228463372	K562	blood:	n/a	n/a
19	GABPA	chr1:228462787-228463430	H1-hESC	embryonic stem cell:	n/a	n/a
20	UBTF	chr1:228463073-228463978	K562	blood:	n/a	n/a
21	POLR2A	chr1:228462462-228464298	K562	blood:	n/a	n/a
22	ELF1	chr1:228462816-228463381	K562	blood:	n/a	chr1:228463333-228463345
23	HEY1	chr1:228463059-228463324	K562	blood:	n/a	chr1:228463294-228463309
24	POLR2A	chr1:228463059-228463140	H1-hESC	embryonic stem cell:	n/a	n/a
25	TBL1XR1	chr1:228463033-228463312	K562	blood:	n/a	n/a
26	ZNF143	chr1:228462836-228463150	K562	blood:	n/a	n/a
27	E2F6	chr1:228462866-228464538	K562	blood:	n/a	chr1:228463368-228463378
28	CBX3	chr1:228462674-228463970	K562	blood:	n/a	n/a
29	MYC	chr1:228463048-228464394	K562	blood:	n/a	chr1:228464133-228464140 chr1:228464032-228464041
30	POLR2A	chr1:228463034-228463888	K562	blood:	n/a	n/a
31	MAZ	chr1:228462906-228464650	K562	blood:	n/a	chr1:228464133-228464140 chr1:228464032-228464041
32	MAX	chr1:228463105-228464537	H1-hESC	embryonic stem cell:	n/a	chr1:228464133-228464140 chr1:228464032-228464041
33	TBL1XR1	chr1:228462966-228463235	K562	blood:	n/a	n/a
34	HMGN3	chr1:228463005-228464399	K562	blood:	n/a	n/a
35	NRF1	chr1:228463041-228463377	K562	blood:	n/a	chr1:228463268-228463279
36	THAP1	chr1:228462933-228463601	K562	blood:	n/a	n/a
37	SIN3A	chr1:228463050-228464420	H1-hESC	embryonic stem cell:	n/a	chr1:228463377-228463388 chr1:228463342-228463355 chr1:228463377-228463390
38	ZMIZ1	chr1:228463038-228463414	K562	blood:	n/a	n/a
39	CTCF	chr1:228463080-228463230	AG09319	gingival:	n/a	n/a
40	CTCF	chr1:228463060-228463210	AG04449	skin:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:228289703..228291795-chr1:228462279..228463838,2	K562	blood:
2	chr1:228353494..228355911-chr1:228462112..228465805,3	K562	blood:
3	chr1:228401876..228404808-chr1:228460949..228463356,3	K562	blood:
4	chr1:228399534..228402324-chr1:228461653..228463776,2	MCF-7	breast:
5	chr1:228395695..228398626-chr1:228460759..228464017,3	K562	blood:
6	chr1:228328463..228331528-chr1:228462308..228464210,3	K562	blood:
7	chr1:228461884..228463852-chr1:228571777..228574496,2	MCF-7	breast:
8	chr1:228461911..228467066-chr1:228644143..228647181,7	K562	blood:
9	chr1:228293306..228296150-chr1:228462712..228464969,2	K562	blood:
10	chr1:228326053..228331395-chr1:228462710..228467617,6	K562	blood:
11	chr1:228461911..228467066-chr1:228644125..228647181,7	K562	blood:
12	chr1:228351819..228355005-chr1:228461791..228464668,3	K562	blood:

Variant related genes	Relation type
ENSG00000269890	TF binding region
OBSCN	TF binding region
ENSG00000181218	Chromatin interaction
ENSG00000143774	Chromatin interaction
ENSG00000196890	Chromatin interaction
ENSG00000162913	Chromatin interaction
ENSG00000143793	Chromatin interaction
ENSG00000181873	Chromatin interaction
ENSG00000162910	Chromatin interaction
ENSG00000154358	Chromatin interaction
ENSG00000203684	Chromatin interaction
ENSG00000270104	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10157289	0.84[ASN][1000 genomes]
rs10157526	0.88[AFR][1000 genomes]
rs10158354	0.82[ASN][1000 genomes]
rs10158680	0.80[ASN][1000 genomes]
rs10916279	0.88[AFR][1000 genomes]
rs10916281	0.89[AFR][1000 genomes]
rs10916299	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12027720	0.82[ASN][1000 genomes]
rs12059144	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12060002	0.84[ASN][1000 genomes]
rs12061320	0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12061490	0.86[ASN][1000 genomes]
rs12061733	0.88[ASN][1000 genomes]
rs12063816	0.89[AFR][1000 genomes]
rs12065660	0.86[ASN][1000 genomes]
rs12066906	0.83[AFR][1000 genomes]
rs12069607	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12081278	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12085738	0.84[ASN][1000 genomes]
rs12089997	0.88[ASN][1000 genomes]
rs16848470	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34673199	0.86[ASN][1000 genomes]
rs35155240	0.81[ASN][1000 genomes]
rs35711644	0.84[ASN][1000 genomes]
rs3795783	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3795785	0.89[EUR][1000 genomes]
rs3795791	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3795800	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3795810	0.82[ASN][1000 genomes]
rs3795811	0.86[ASN][1000 genomes]
rs3795814	0.82[ASN][1000 genomes]
rs56852844	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs573128	0.84[ASN][1000 genomes]
rs60608705	0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs61825280	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61825285	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs61825312	0.86[ASN][1000 genomes]
rs6660457	0.90[AFR][1000 genomes]
rs6694419	0.90[AFR][1000 genomes]
rs6694442	0.90[AFR][1000 genomes]
rs9787095	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv32853	chr1:227880116-228806209	Enhancers Genic enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	187 gene(s)	inside rSNPs	diseases
2	nsv826908	chr1:227895386-228691100	Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	157 gene(s)	inside rSNPs	diseases
3	nsv523935	chr1:228038124-228681749	Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Weak transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	137 gene(s)	inside rSNPs	diseases
4	nsv873253	chr1:228231601-228537942	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
5	nsv873254	chr1:228231601-228543800	Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
6	nsv873255	chr1:228254753-228684779	Genic enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	133 gene(s)	inside rSNPs	diseases
7	nsv827019	chr1:228314167-228651020	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	106 gene(s)	inside rSNPs	diseases
8	nsv1012078	chr1:228340876-228521843	Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
9	nsv535320	chr1:228340876-228521843	Active TSS Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	63 gene(s)	inside rSNPs	diseases
10	nsv873263	chr1:228391808-228494790	Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	nsv873264	chr1:228423647-228543800	Flanking Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
12	nsv873265	chr1:228434395-228525008	Active TSS Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
13	nsv873266	chr1:228434395-228537942	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
14	nsv873267	chr1:228434395-228585837	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
15	nsv873268	chr1:228442663-228537942	Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
16	nsv873269	chr1:228442663-228543800	Strong transcription ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
17	nsv873270	chr1:228442663-228699477	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
18	nsv1009891	chr1:228450763-228742676	Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Weak transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
19	nsv873271	chr1:228450868-228470995	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
20	nsv873272	chr1:228450868-228538968	Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
21	nsv873273	chr1:228450868-228556788	Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
22	nsv873274	chr1:228450868-228585837	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
23	esv1798020	chr1:228456147-228556788	Strong transcription Bivalent Enhancer Weak transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
24	esv1818776	chr1:228456147-228556788	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
25	nsv873275	chr1:228456147-228585837	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
26	nsv517545	chr1:228456147-228685999	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
27	nsv873276	chr1:228456943-228585837	Weak transcription Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
28	nsv1013500	chr1:228459134-228849601	Flanking Bivalent TSS/Enh Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
29	nsv827064	chr1:228459934-228469437	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:228445000-228463200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr1:228455400-228484800	Weak transcription	A549	lung
3	chr1:228456400-228485800	Weak transcription	Hela-S3	cervix
4	chr1:228456600-228463200	Weak transcription	Aorta	Aorta
5	chr1:228457200-228472000	Weak transcription	Fetal Heart	heart
6	chr1:228459800-228469600	Weak transcription	HSMMtube	muscle
7	chr1:228461800-228463400	Bivalent Enhancer	Placenta	Placenta
8	chr1:228462400-228463200	Enhancers	Gastric	stomach
9	chr1:228462400-228463200	Enhancers	Spleen	Spleen
10	chr1:228462400-228464200	Weak transcription	Dnd41	blood
11	chr1:228462600-228463400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr1:228462600-228463400	Flanking Active TSS	Stomach Smooth Muscle	stomach
13	chr1:228462600-228464400	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr1:228462800-228463200	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr1:228462800-228463200	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
16	chr1:228462800-228463200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
17	chr1:228462800-228463200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
18	chr1:228462800-228463200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
19	chr1:228462800-228463200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
20	chr1:228462800-228463200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr1:228462800-228463200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr1:228462800-228463200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:228462800-228463200	Flanking Active TSS	Colon Smooth Muscle	Colon
24	chr1:228462800-228463200	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
25	chr1:228462800-228463200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
26	chr1:228462800-228463200	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr1:228462800-228463200	Flanking Active TSS	K562	blood
28	chr1:228462800-228463400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
29	chr1:228462800-228463600	Flanking Active TSS	Primary T cells fromperipheralblood	blood
30	chr1:228462800-228463600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
31	chr1:228462800-228463600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr1:228462800-228463600	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
33	chr1:228462800-228463600	Flanking Active TSS	Duodenum Mucosa	Duodenum
34	chr1:228462800-228464000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr1:228462800-228464200	Active TSS	H9 Cell Line	embryonic stem cell
36	chr1:228462800-228464200	Active TSS	NHEK	skin
37	chr1:228462800-228464400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr1:228462800-228464400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr1:228462800-228464400	Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr1:228462800-228464400	Active TSS	Fetal Kidney	kidney
41	chr1:228462800-228464400	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
42	chr1:228462800-228464400	Bivalent Enhancer	Stomach Mucosa	stomach
43	chr1:228462800-228464600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr1:228462800-228464600	Flanking Active TSS	Adipose Nuclei	Adipose
45	chr1:228462800-228464600	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
46	chr1:228463000-228463200	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
47	chr1:228463000-228463200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr1:228463000-228463200	Flanking Bivalent TSS/Enh	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr1:228463000-228463200	Flanking Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr1:228463000-228463200	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell

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