| Tag | Content |
|---|
EnhancerAtlas ID | HS091-16099 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:3739450-3740820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:3740614-3740633 | TGGCCACCAGAGGGGGCAA | + | 6.12 | | Lhx3 | MA0135.1 | chr16:3740331-3740344 | AAATTAATTAGTT | + | 6.29 | | TBX20 | MA0689.1 | chr16:3740713-3740724 | TTTCACACCTA | - | 6.14 | | TBX2 | MA0688.1 | chr16:3740713-3740724 | TTTCACACCTA | - | 6.32 | | Zfx | MA0146.2 | chr16:3739488-3739502 | CCCGCCTCGGCCTC | + | 6.01 | | mix-a | MA0621.1 | chr16:3740332-3740343 | AATTAATTAGT | + | 6.62 |
|
| | 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 |
| GH16I003689 | chr16 | 3739703 | 3742199 |
|
Enhancer Sequence | TAGCCAGGAT AGCCTCGATC TCCTGACCTC ATGATTGGCC CGCCTCGGCC TCCCACACAT 60
TTAAGATCAT GAACAAAAAG AAAGAAGCAG ACAGAAACAA AGTCTGGCTG GGCACCATGG 120
CTCATGCCTG TAATCCCAGC ACTTTGGGAG GCCAAGGCAG GAGAATCACT TAAGCCCAGG 180
AGCTCAAGAC CAGCCTGGGC AACACAGAGG GATCCCGCCA TCTCTACAAA AAATACACAA 240
AGTAGCTGAC GGTGGTGGCA CACACTTGTG GTCCCAGTGA CTCAGGGGGC TGAGGTGGGA 300
GGATCACTTG AGCCAGGGAG GTCGAGGCTT CAGTGAGCCA TGATTGCACT ACAGCACTCG 360
GCCTGGGTGA CAGAGAAAGA CCCTGTCTCA AAACAAAACA AAACAAAAAG TCTCTCAGAA 420
AGGAGGTCTC AGGGCAGGAC AAATCCTCCC ACTGCTGAGG CCAGACATGC CTCGGGCTAT 480
GTCGAGGGAA TGCTGAGCCT GGTTTCCCAA TGTGCATGGT TACGAGAACT GGACTGCCTC 540
TAAGAACCAG ATTATATGTT CTTTCTTTTT TTTTTAGAGG CAGGATCTGG CTCTGTTGCC 600
CAGGCTGCTA TGCAGTGGCA GGATCGTGCT CACTGCAGCC TCAACTTCCT GGGCTCAACC 660
GATTCTCCTG CCTCAGCCTC TCAAGTACCT GGAACCACTG GTGTGTGCTA CCATGCCTGG 720
CTAACTTTTT AATTTTTTTC TGTAGAGAAA GGGTCTATCT TGCCCAGGTT GGTCTCGACC 780
ACTTGGCCTC AAGCAATCCT CCTGCCTCGG CCTCCCAAAG TGCTGGGATT ACAAGTGTGA 840
GCCACTGTGC CTGGACTATA TTCTTCAAAA AAGCGGTTTC CAAATTAATT AGTTAGAAAT 900
CAAAATAACA AGAAAACCTC ACTTCTCTTT TTAACTTCAA AGATTCTACT CTTGTCGACC 960
CACTTAAAAG CCAGAAATGG AGCCACTTCA GGACTGGCTC CAAAGACTGC TTTTTTATAC 1020
TTCAGAGGGA ATGAAAAGAC AGCTCCAGAA TTCGGTCCTG CGCAGACTGG GCCAATGCTG 1080
AGTTTCCCCT CCCGCTTCCA TGATTATTAG CAGATGTGCC ATGAATCACC ACTCAGGGGA 1140
GGTGCCGGAC GGCAAACTCA CGGGTGGCCA CCAGAGGGGG CAAGACACAC CCGACACTGG 1200
CAGAAGTCCC TCGCTGGGAC AGAAATGGAG GGCGCAGCAC TCCCTACAGC CAAGACCTTC 1260
TGATTTCACA CCTAAGGCGG TGGCTCTACC AATCACTGCC TCCACCCTGA AAATGCCCCT 1320
TTACGCACAG CAGTGAACCA AAAAGCCCTC CCAGACCAAA GCACGAGCCA 1370
|
