| Tag | Content |
|---|
EnhancerAtlas ID | HS098-46320 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:139620670-139621850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr5:139620878-139620899 | GGAGGCTGGGGAGAAGGGGAA | + | 6.19 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_23431 | chr5:139619202-139622461 | Colon_Crypt_1 | | SE_24605 | chr5:139619874-139621889 | Colon_Crypt_2 | | SE_28509 | chr5:139619582-139623682 | Fetal_Intestine | | SE_31400 | chr5:139615731-139623973 | Gastric | | SE_41163 | chr5:139618857-139623978 | Left_Ventricle | | SE_43055 | chr5:139619856-139623214 | Lung | | SE_48219 | chr5:139618750-139623208 | Psoas_Muscle | | SE_51117 | chr5:139619841-139627183 | Skeletal_Muscle | | SE_53259 | chr5:139619243-139622195 | Small_Intestine | | SE_64598 | chr5:139620246-139621701 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I140239 | chr5 | 139619055 | 139627656 |
|
Enhancer Sequence | GCCTGGGAGT AATGAGTTCA AAGTCCCTAG TTCCCCACGT TTCCAAGTAT GTTATGTGAA 60
AGCCCTGGCA AGAACGAACC TGATTAAACT GGAGGAAAAA GGTGGAGCAA GCAAGACTAG 120
GACGTTTTTG TTTCCCCAGT TAAGCTGCCT GAGGTTCAGG GGCTCTGACA GGTGAGAAAG 180
GCATGGCCAC CGCCTCAGCC CTGTCTCTGG AGGCTGGGGA GAAGGGGAAG CAGTGAGGAG 240
ACTGACTGAT GTCCTGATGC CCATGCCCCA CACGGCGGTC ATGAAGACTG AGTGGCCCCA 300
TGTCCAGAAA GCCCTCAGCA CAGGGCCTGG CACTTGTGAA TACCTCAATA AATGGTAACT 360
TAAGAGAGCC TGTGAGGCCC CTCCCACTGC AGCCAGCCTC CAGCTGAGTC TCTGGCCTGA 420
AGCCCAGGGA TGGCCTGCAC ATGAATCAAG CAGGCTATTT CCAGAGCTGG CAGGGGAGGG 480
GCTTTCTGTC CCAGGGGCAG GCGAGCCAAT CCTGTGACAG GGAGAGCACA GGGAAGGGGT 540
TATTCAAGGG GATCTGCATG CCATTGTATT CTGGTTTCCC TGTCCAGAGC TGCCCATGCA 600
GGATCCCGGG GTGGGCAGGC CATCCAGGCA GATGGAAGGG ACACTCTGCC TGGGGCTTTC 660
CTGCTGCAGT GACCCCAGGG CCTGGGGTGG CCAGGCTTCA GTGGGTAGGG TAGGCTCTGG 720
CTGGATGTGA GAGATGACTT TGCTGTAGCC CCAGTCACCT CTGTTCTCTT TCTGATCCCT 780
TTTCTATCCC AGTTGGGTAT GAGCAAGCCT GGCTTGCCAG AGGCTTTAGA GCCATAAAGG 840
CCTGGGTTCG GATTCTGCCC TTGCCTCTGC CTCGTCACAT GTGCTTGAAC GAGAGACTTG 900
AGCTCTCTAA GCCTCGAATT CCTTGCCTGT GAAGTGGGAA TGATGGTAGT ATCTACCTCA 960
GGGTTGCTGT GAAGACGAAA TCAGGTACTT GACCTTAGGA GGCCTCAGAA TAAATGAGCC 1020
ATTCATCCTC TCCCTCTGAG CAGGCTTTCC TGGTGAAGGG CATCTAGACC CAGACCTGTG 1080
CTGCTGAGTG GAGCCAAATG CAAGTGGACT AGGATTAAAC CTGTGCCATA GGAGAAGGAA 1140
AAGGAACATG TCCGTGCAGT AGAGGGCAGC TGATACAACG 1180
|
