| Tag | Content |
|---|
EnhancerAtlas ID | HS091-32332 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr21:45929810-45932100 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr21:45930540-45930559 | CGCCCAGCAGGGGGCGCCG | + | 7.28 | | KLF16 | MA0741.1 | chr21:45930760-45930771 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr21:45930761-45930771 | GGGGCGGGGC | - | 6.02 | | NFE2L1 | MA0089.2 | chr21:45930988-45931003 | CACTGACTCAGCAGA | + | 6.01 |
|
| | 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 |
| GH21I044510 | chr21 | 45930046 | 45931530 |
|
Enhancer Sequence | GTACCTCTCG AGTTTTCTCT TACACGCTTT CCCTGGCCTT GCAGTTTGGC TGAGTCTTTC 60
CTCTGGCTCT GTAGACAGAA GCCATCTCTG GGTTCCTGTG CTTGCCATTC CTCCATAAAT 120
CACTTACCAC CGTCAAGAGG CAACAGGTCT GGGGCTGCAC ACGGAGGCCC AACTGCGGCA 180
CCTCTGCCAC CAACCTTGAG CTGCAGGACT GTCTGCATGT GGGGTCCACA AGGCGGAAGC 240
TTCTGCCAGC ACCTTGGGGA TAAGGGTGGT GGGGCTGCAC GGGGAAGGGG AAGGCTGCTT 300
CCCTGGGGAC AGTGTCCCCA CAGGCCGGGG ATCCCTGCGC ACGGTCCCAG GCTGTCCTAG 360
CTGAGGACGG AGCCGGTCAT GCTGCGGGGC TGTGTCTCTT CCTGACTCAC CCCCGTCCGG 420
AGGGCCTTCT GCCTGAGGGA CATTGCACCA CCGGGCCAGG TAAGAAGCAG CTCTGAGAGC 480
CTCCCGTGAC AGCAACCACT GGGACGTTTT CTATTTGCCC AAATCGACCA GCAAGGGCCC 540
GGCTCAGACG CCCCTGGGTC TGATGCGACC TGCCCTCCGC AGCAGGTCAG GCACCCTCCC 600
TTGCTTGTAT GCTCAGGACG GGGCTGCCCA GGCATCTTCT GGTCCCCCTG ACTGTCCGGC 660
GCCTGCCCGG CCGGCTCAGG TGCTGCAGGA AAGAGAAAAC TCTGGGCCCA ACGTCAACGT 720
GCGTTCTCCA CGCCCAGCAG GGGGCGCCGT TGCCCGCCCG AGCCCGGAGA GCCTGGGCTG 780
CAGGGGAGGG CGCCACAGGT GAGGACACAG CTCCGTGGGC ACCAGGCAAG GTCCCAAAGC 840
AGATCCGCAG CCGGTCAGAG GAGCGCACAT GGGTGAGCTT AAGCTAAGAA AGCAAGACTC 900
ACTAGGCAAG GACAGGGGCC CAGGACACCT GGCGGCGCCG AACCCTCGGC GGGGGCGGGG 960
CCGGGGGCTG GCTGAGGCTT TCCCGGGTCA GCGCGCCCTC CCCTCCTGCA GCTCCACGAG 1020
ATGTGACTAT TCCTATCTGC TGGAGAACAG CCGTCCAGGG CCACCCCACG TCCTTCAAGG 1080
GGACTCTGAG ACACTCTGGG CCGGTGGGAC CTTCAGCAGC ATCTGGACTT TGGCTGCCTC 1140
ACAGGTGGGC GGGGGGGAGT GTTACACACA GGCCAGTTCA CTGACTCAGC AGAAGAGAAA 1200
CAGGAATCAT CAGACTGTTC AACCCTGGGC TCCTCCCACG CCTGTGCTGA GGAAACCAAC 1260
TGAGTGGGCA ACCCTCACGT GTGTACACAT GCCTGCACAC ACCTGCACAC ACAGGCCCAT 1320
ACCTGCACAC CTGCATGTAT GCATACATAC ACAAACATGG ATGTGCACTG TGCGCACACA 1380
CACATGCACG CCTGCATGCA TGCATACACA CACAAACATG CATATGCACT GTGTACACAC 1440
ACACATATAT GCTTACATTT TTACATGCAC AGATGCACAT GCATGCCTGT ACACATGTGG 1500
ATACACATGC AGATACACAG GCCTGCTCAT GTATACATAC ACATGTATAC CTACACACAC 1560
GTATGTATGC ATGCAACCAT GCATCTGTGT CCATGTGCAT ATGTGTATAC TTGCACACAT 1620
GCCTGTACAC AGGCAGATCC CTGCAGGCAC ACCCATGCAT CCGCCTGCAT GACATCTACA 1680
CACACACATG CACCCACACA GCACAGCTCT CCCCACATTG CTGGAAAAGA CTGAGGACAC 1740
ACGCCTCCAG CCCTGGGCGT CCTTCCAGTG GAGCCCCTGC TTCTTAGCTA CTTGCTGATG 1800
CTCACCTGTG TTGAGGCAGA TCCTGATGGA CTGCCGGGGC CAGAACAGCC TGAAACTCCC 1860
TCTCAGGGAA AGGCCCGGAG TGCCCGCCCT GTAGCAGCCC AGGGTGATGG GGGACCCCGA 1920
GCTGGCACTC AGCACTGTGT AGAGAGAGCT TTACTGCAAG TTGGGGCTGA GCCGGGCATC 1980
ACATCTCAGT GATGAGTGAG GTGCCCTCCC TGCCCAAAGG AGCCCTGGAA CGGGCTGCTG 2040
CAGATGGGGG ACCATGGAGG GGCTGCCCGG GGCCTTGGGG GCACAGAGGA AGAGGGCCCA 2100
AAGGCATGGA GGACGGACAG GGGAGTTGGC AGCAGGAAGC AGGGAAGGGT ATCCAGGCAG 2160
AAGGAACTGC AGGACAGACA CACAGGACTG AGGGAGCCAG GAGGGCTGGG CGCACACAGA 2220
GTGCGGAGCA GGGGCTGGGG CGGGCCTACA GGGCCTGGGT GCTGTGGAAA GCAGCTGGGC 2280
CTCCAGGCAA 2290
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