| Tag | Content |
|---|
EnhancerAtlas ID | HS092-00996 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:31567150-31569720 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr1:31568446-31568461 | GGGTCACAGAGACCT | + | 6.22 | | PPARG | MA0066.1 | chr1:31568444-31568464 | CTGGGTCACAGAGACCTCCT | + | 7.01 | | TFAP2A | MA0003.3 | chr1:31567538-31567549 | AGCCTGAGGCG | - | 6.14 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I031094 | chr1 | 31567567 | 31568417 |
|
Enhancer Sequence | CAAAAAAAAA AAAAGAAAAA AGAAGGAGAA GAAAATTAGT GGGGTGTGGG GGCATTCCTC 60
TGTGGTCCCA GGTACTCAAG AGGGTGAGGT AGGAATGGAT CACTTGAGCC AGCGAGGCAG 120
AGGTTGCAGT GAGCCCAGAT GGTGCCACTA CACTCCTGCC TGGGTGACAG AGTAAACCCT 180
GTCTCAAAAA TAAATAAATG CATACATACA TAAATACATA AATAAATGCA AGAAACTTAT 240
TTTTCTCTAG ACAGCAGGGC AAATTTCTTT TTTTTTTTTT TTCGGTTAAA TTCGTCCAAT 300
ATTTGTTGAA TTGTGAATGG TTGCAAACGT TGCTGCAATC AGAGACTCAC CCATCCTGTT 360
GCCTCTCCTG GCTTCCCTTT GAGAAGGAAG CCTGAGGCGG GACATCCCCC AAACTCTGGG 420
AGACAACTGG GGAGACATGG GGTATGCATA GAGATATGAT GAAATCGGGG AACAGGTAGG 480
GCGGTGTGGA TTCCGGGGAA GACACATACA AACAGACTCT ACCACACAGA GGTAAAGACC 540
AGGGGTGTCA ACCTCTGCCC CCAACAGCAG CTGCGAGAAC AGGGGAAGAC CAGGCGTCCA 600
TGAGACATTT CAGTTCTTCC TGTCATGAAG CATCTGCTGA GAGGAGCTGG GTCAAGGTCC 660
CTGGACTCTG CCTTCAGGGC ACATTAGCCC TGAGCCAAGG CAGCTTTGAT GGCAGCCACC 720
AGCTTCAGAA ACTTGTTTTC TGTGTCCACA TAGCCATCAC CTTTCTTCTT AGAGTGAATC 780
AACTTCCCAG CTACCATTAC GTCAAAGAAC CCGGTGGCCT GGGGAGTTCC CTTGCTGCAG 840
ATGTCCAAAG TCCAGAGGAA CTCATCTTCT TTTTCTTTTT TTTTCTTTGA GATGGAGTCT 900
CACTCTGCTG CCCAGGCTGG AGTGCAGTGG TGCGATCTCG GCTCACTACA ACCTCGACCT 960
CCTGGGTTCA AGTGATTCTC CTGCCTCAGC CTCCCAAGTA GCTGGGACTA CAGGCGCCCG 1020
CCACCGTGCC AGGCTAATTT TTTTTGTATT TTTAATACAA ACGGTGTTTC ATTATGTTGG 1080
CCAACATGGT CTCGAACTCC TGACCTCATG GTCTGCCCAC CTTGGCCTTC CAAAGTGCTG 1140
GGATTACATG CGTGAGCCAC TGTGCCGGCC GGGGGAACTC ATCTTCTAAC TTCTTCTTGA 1200
GCTGAAGATA CTTGGACTTG TAGCCTCAAG TGCCACATAA ACCACTCGCG AGAGCCATGG 1260
CTCTGGGCTG CCACCCTCGC TGGGGAGCAG AGACCTGGGT CACAGAGACC TCCTGCCTGG 1320
ACGCATGAGG TCTGCACCAC AAATTTATTT AAAAAGGAAT TTTATTCATT TAAAATATAT 1380
GCATACAGTT GCTTACTATA ATCTAGGCAC TGTCTTAAGC ATTTGTTTCC ACCAGCTACA 1440
CTAAATGACT CATCTACATC ACCAGATTTC AGGAGAAATT AGATGCACTG CCAGAAGAAA 1500
AGGAAATACT TTAGATACTA GTTTTAGCAA AACATGGCAT TAATACATTG CAGATGGAGC 1560
AGGATGTGAA TTTACCTACA ACTTCCACAC TCTGTAACTG ATGGATTTTG AGAAAAACTA 1620
GGAAAAAACA GTGACAAAGA ATTCATTAAA CCAAATTACT TTTTGACTAT ATATCTACTT 1680
GGCCACATAA TTTTGCATAT TAAACAGCAA CTGTAGTTAA AATTATCTAT CTCAGATAAG 1740
AATCTTTTTC TTTTTAGTTT GTATGTATGT ATGTATGTAT GTATTTTGAG GCAGGGTCTC 1800
ACTCTCTTAC CTAGGCTGGA GTGCTGGAGT GCGATCACAG CGCACCGAGG CTTTCCCTCC 1860
CAGGCTCAAG TGATCCTCCC ACCTCAGCCT CCCCAGTAGC TGGGTACACA GGCAAGGATC 1920
ACCACATCTA GCTAATCGTG TTACTTTGTG TAGTGACAGG TTCTCCCTAT GTTGCCCAGG 1980
CTAGTCTCGA ACTCTTGGGC TCAAACAATC CTCCTGCCCC AGTCTCTCAA AGTGCTGGAT 2040
TACAGGCATG AGCCTCTGTG CCCGGTCTTT TTTTATTTTA GGTATTTTTG TATTTATTTA 2100
TTTTTGAGAC GGAGTCTTGC TCTGTCACCC AGGCTGGAGT GCAGTGGCAC AATCTCAGCT 2160
CACTGCAAGC TCTTTCTCCC GGGTTCACAA CATTCTCCTG CCTCAGCCTT CTGAGTAGAT 2220
TGGGACTACA GGCGTCCGCC ACCACGCCCA GCTAATTTTT TTGTATTTTT AGTTGACACG 2280
GGGTTTCACC GTGTTAGCCA GGATGGTCTC AATCTCCTGA CCTTGTGATC CTCCTGCCTT 2340
GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GAGCCACTGT GCCCGGCCGC CTTTTTTTTT 2400
ATTAATAAGA GATGGAGTTT TGCTTAATTG CCCAGGCTGG TGTGCAGTGG TCTGATCATG 2460
GCTCACTGCA GCCTTGAACT CCTGGACTAA AGCAATCTTC CTGTTCCAGC CTCCCCAGTA 2520
CCTAGGACTA CAAGCATGTG CCACCACGCA GGGTGATTTT TAAAAATCTT 2570
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