| Tag | Content |
|---|
EnhancerAtlas ID | HS091-00723 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:21557970-21559320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:21558635-21558654 | AGTCCACCAGGGGGCACCA | + | 7.48 | | Nr2f6(var.2) | MA0728.1 | chr1:21558053-21558068 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 21558552 | 21558736 | | chr1 | 21558408 | 21558927 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I021232 | chr1 | 21558552 | 21558736 |
|
Enhancer Sequence | ATTACAGGTG TCTACCACCA TGCGTGGCTA ATTTTTGTAT ATTTAGTAGA GACGGGATTT 60
CACCATGTTG GCCAGATTGG TCTTGAACTC CTGACCTCAA GTGATCTACC CGCCTTGGCC 120
TCCCAAAGTA CTGGGATTAC CGGTGTGAGC CCCCGTACCT GGCCAAGAAC TCTATTTATG 180
TATTTATTTA TTTTAGAGAC AGGGTCTTGC TCTGTAGCCC AGGCTGGAGT GCAGTGGTAC 240
AACTGTAGCT CACCGCAACC TCAACCTCCT GGGCTCAAGC GCATGCTACC ACGTCCAGCT 300
AATTTTTTAA ATTTTTTGTA GAGATGGGGT TTCACCATGT TGCCCAGGCT GGTCTCAAAC 360
TTCTGAGCTC AAGAGATCCT CCCACCTTGG CCTCTCAAAG CGTTCGAATT ACAGGCGTGG 420
GCCGCTGTAC CTGGCCATAT GGAGGAATTT AAAACATCAT ATTTATATTC AAATAATCAC 480
AAATACTTCA ATGGGTAGGC AAGGAAATTT AAATAAAAAC ATTCAAGCTA AGTTAAAATA 540
CTTCAGATAA ACTGGCAACA GAGCCTATGC CATGTTCTGA AGGTAAAAGC CCACCTTCTT 600
GTACATAGCG GGGTGTCCTG GTTGGAGGCT GGAAATGAAG GAAATAGAGA TGTTTGAACC 660
CCTATAGTCC ACCAGGGGGC ACCAGAGGCA AAGAGAAGTT GATTGCACCC TTCCCTAAGA 720
TTTATCCCAA ATGTTTGCAC TGAGGAATGG AAGGACCTTG GACTGAAGAC TGGAACTGGG 780
CTGACTACAT CTAATTTTTT TGAGGAGACA GTTTTTTTTT TTCTTTCTTT CTTTTTTTTC 840
AGGCAGGGTC TCGCTCTGTT GCCCAGGCTG GAGTACAGTG GCATGATCTT GACTCACTGC 900
AGCTTCGACC TCCTGGGCTC TAGTGATCCT CCCACCTCTG CCTCCCCAGT AGCTGGGACT 960
ACAGGTTCGT GCCACCACGT CCAGCTAATT TTAAAAATTT TTTGTAGAGA CCACATCTCC 1020
CTATGTCGCC CAACCTGGTC TTGAAGTCTT AGGCTCAAGC GATCTGCCCA CCTCAGCCTG 1080
CAAAGTGCTG GGATTGCAGG CCTGAGCTAC TGTGATTGAC CTGAGGAGAC AGTAATAAAA 1140
AGGACAAAGA CCAGGTCTCA TTCTAGGTTA TCCTGATTTA AGGTCAGGAA GCTGTATTTT 1200
TTTTTTTTTT TTGAGATGGA GTCTTGCTCT GTCACCCAGA CTGGAGTGCA GTGGCACGAT 1260
CTCGGCTCAC TGCAACCTCC GCCTCCCGGG TTCAAGCAAT TCTCGTGCCT CAGCTACTCA 1320
CTCCTGAGTA GCTGGGACTA CAGGTGTGCG 1350
|
