| Tag | Content |
|---|
EnhancerAtlas ID | HS091-11183 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:122689230-122690860 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr12:122690452-122690470 | GAAATGGTTTCACTTCCC | - | 6.54 | | Zfx | MA0146.2 | chr12:122689471-122689485 | GAGGCCGAGGCCGG | - | 6.28 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 122690114 | 122690363 | | chr12 | 122690389 | 122690785 |
|
Enhancer Sequence | GGTCAGATTC TTTCACCGCC TCTGCCAGAC CCCCTTGTCC CCCACCCCCG CATAGATCTC 60
CAGGGGGCTC AGAAAACTCT GGCCGGTGGC TCACGCCTGT AGTCCCAACG CTTTGGGAGG 120
CCAAGGCGGG AGGATCGCTT GAGGCCAGGA GTTCCAGACC AGCCCAGGCA ACAAAAGATA 180
CCACATCTCT ACAAAAAATA AATTAGCCGG GCCCTGCACG CCTGTAGTCC CAGCTACTGG 240
GGAGGCCGAG GCCGGAGGAT CGCTTGAACC CAGGAGTTCC AGGCTGCAGT GAGCTATAAT 300
TGTGCCACTG CACTAGAGTC TGGGTGACAG AGACACTGTC TCAAAAAAAA CCAACAAAAC 360
CCTTAGCTCT TTCACTAGCC GGGCTGGCCT CTTCCTACTG TAAACCTGCT GGGCCCCCGT 420
CTCCCTTCTT TCTCCCCTCT CTCCTGCCCT GGAGCTGCCT GACTCTGCCC ACGGCCTGCA 480
GAGACCCCAG GTCTTCACGC AAGGTGCCAT TCCTCACTCA GTTCTTGCTC AAACGTCCCT 540
CCATCAAGGA GGGCTTTTTA GCTACCCTTG GCTATGGGAT CCGTCCTCCG CGTCAGCCAA 600
TTCTCTGCAT TAGACTGTAA CTTCTCAACA TACCTGGTTC CTATGCGTTT TGTGCTCCCC 660
TCTGAGAGGG CAGCGACCCT GTCTTGCTTG CCACTGCATC CCTAGCACCT AGCAGTTGCT 720
TTTCTGGTGA CGGCGGCTGT GGCAGTGGCC AATGCGGCAG ACTGGTCAGA AGTGAAGGGA 780
CAGGATGACT TGGCAGTGGA GGTCAAGGGG AGGGGACTGG GGCAGAGGGA GACACCAGAG 840
GGACAAAAAT GAGAAACTGA AGACAGGCTT TGCTACGTGG AGCTCGGGCA GGCCACACTG 900
GTGGATTCTG TCTCCTCATC CTTCTTTTCA GGTCCCTGGG AGAAATCAGC ACTTAGAACG 960
TGGTGGGAAG GCGGGGCGGG GTGCCTCGGA AGCCATCCCT GATACAAGTC CCCAGCTTTC 1020
CTGCTTCCCC TCTTGTGGTG TGTGGCTTTG TCTCCCTCCC TCCCTCCTGG AAGCCCCGAC 1080
CTCTGAGGCA GGTGTAAAGG GTGTGTGCTT TGGTGGCCAC GGCCACCCTG TGGTGCTGGT 1140
TCTCCTCCGA GGGAAGCAGT GCACTCCTGG TCATCTTGGA GACGCCCAAC ACAGGACCCC 1200
ACAGGCACCA AGCTTTTTTT GGGAAATGGT TTCACTTCCC ACTTGAAAAG CCCTGAATGT 1260
CAGTTCCACA CTTAGTGAAT TTGATCCAAG CTAAACTGAG TCTGTGCCTA AAACTCATCA 1320
GGTGCTCGAG TTTCCTGGAA GAATGGCTGG GAACGTTTAT GGTGTCAGCT GTAAAGTGGC 1380
TGCAAGTCCT TTTGGGAAAA ACAGACCCAG GAGTCCTCAG ATGATGGCAG AGGAGGGCAA 1440
GGGCTGGCAA AGCAGCTGTG CTTAGCCCAT CCTCAGGGGA GGGAGGACTC TGGAAAGAGC 1500
CTGAGGATAC GCTGAGAATA AAAAGTCCAG AGGCCAGCAG GGACTTAGCG GCTGGGGTGC 1560
AGGTTAACTC CTGCCCAACT CTTGGGGACA GGGACCCGGG GCTGGGCCCT GCTCAGGTGG 1620
CTCTCTCCTT 1630
|
