| Tag | Content |
|---|
EnhancerAtlas ID | HS007-04086 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr12:105042530-105043770 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:105042768-105042786 | CCTGCCTCTCTTCCTTTC | - | 6.21 | | EWSR1-FLI1 | MA0149.1 | chr12:105042764-105042782 | CCTTCCTGCCTCTCTTCC | - | 7.6 | | ZNF263 | MA0528.1 | chr12:105042764-105042785 | CCTTCCTGCCTCTCTTCCTTT | - | 6.06 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09142 | chr12:105027432-105048804 | CD14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 105042709 | 105042954 | | chr12 | 105043287 | 105043477 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I104648 | chr12 | 105041780 | 105046577 |
|
Enhancer Sequence | GCAGTGAGCC GAGATCACAC CACTGCATTC CAGTCTGGAC AACAGAGCGA GACTCTCAAA 60
AAAAATAGAA AAGAAAGATC TGAGCAGGGA CTAGCAAACC AGCAAGATCT GAGGCACCCT 120
GAAACTGGCA ACAGAGATGA GCCATTGTCA CCCTGAGGCC TGAAGAGCCG GGGTGACAGC 180
TGCCTGAACT GCAGTGGAAG CAGGGGAAAT ACACCCTTAC TCCAATCAAC CTCCCCTTCC 240
TGCCTCTCTT CCTTTCTGTC CTCTTGCTGG TTCCTCCTGT TGGCCAAACT GAAACAGAGG 300
TCAGCCAGCT GCCAGCATGG AGCCCGGCTG ATGTAGGATG GGAATCAGCC TCAGGGATGG 360
GGGAAGCAGA GTAGAGAAGG GTGGGGAATG GATGGGGCTA GGGGTGGGAA AATGAGGGAA 420
TGGGAAAGCC AACACATTCA GTCAATATTC TTGGAACATC ATTAAGACAC AGAACAGTGT 480
ATCGGAACAG AGGTTACTGA CTCCTGCCCT ATTGTAGATC TGGGGTAATT TTATTATTAA 540
TAATAATCTT AACAGCAATA TTAGCTATCC TGTGTTAAGT CTTTTCCATG TACAGGGCAT 600
TGTATTACAT TACAGGGCAT TTAACACATA CAATTTCTAA TCTTTACAGC CAATCTGTTA 660
GGCACATGTT ATTATGAGTC TCTTTCAGGC AAGGAAAAAT GAGTTTGGAA AGGCTCAGTA 720
TCTGCCTGAG GTCACAAAAT CTGTAGTAGA GCTAGGATTA AACTCAGGTC TGTTTTACTC 780
TAAACTCCAA GTGCTTCTGT CTAAAAGCAG TCTAGACCAA CCTAAGGGGG AGTAGGCGAA 840
CCAATGTGGT TTCTGTATGA AGCTTTCAAT GCCTTCTTCC ACAGTGGAGC AATAATTTTA 900
AAAAGAAGAA GGAAGAGAAG AAAATCTTTA GCATGCCAAC TCATCTGAAC AACTGCCCAG 960
GAGTCAGAGT ATAGTGTGTT TGGCAAATTA TGAGTTTTGT GTCAGTGCAT ACAAAGTAGG 1020
CAAGAAGTGA GGAAAAGATC CCTTGAAATA ATGGGATGGG GAATGCAGCA CTCAGCATGG 1080
TGAGCTCACA TAATAAAGTC ACCTTGGAGA GCTCAGTAAA TTATTGTGCA GAGACTGCTG 1140
CTGATAGACG AGGCACACTG GCATCCCTCA GTGCCCCTGG TGGCTCTGAA AACAGTGCCC 1200
TGGCAGCTCT GGGCACCCAA AGGGCACTCC ATCAATTACT 1240
|
