| Tag | Content |
|---|
EnhancerAtlas ID | HS047-18051 | Organism | Homo sapiens | Tissue/cell | Fetal_placenta | Coordinate | chr19:53369510-53372180 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr19:53369541-53369552 | AGTGACTCATG | + | 6.14 | | LMX1B | MA0703.2 | chr19:53370416-53370427 | GATTTAATTAA | + | 6.02 | | Lhx3 | MA0135.1 | chr19:53370420-53370433 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr19:53370424-53370437 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr19:53370428-53370441 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr19:53370432-53370445 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr19:53370421-53370434 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr19:53370425-53370438 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr19:53370429-53370442 | AATTAATTAATTA | - | 6.78 | | Lhx3 | MA0135.1 | chr19:53370433-53370446 | AATTAATTAATTT | - | 6.92 | | Lhx3 | MA0135.1 | chr19:53370417-53370430 | ATTTAATTAATTA | - | 6 | | NFE2L1 | MA0089.2 | chr19:53372088-53372103 | TGTGCTGAGTCATGA | - | 6.8 | | Nfe2l2 | MA0150.2 | chr19:53372090-53372105 | TGCTGAGTCATGATG | - | 7.77 | | Nr2f6(var.2) | MA0728.1 | chr19:53370669-53370684 | TGAACTCCTGACCTC | - | 6.22 | | POU6F1 | MA0628.1 | chr19:53370422-53370432 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr19:53370426-53370436 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr19:53370430-53370440 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr19:53370434-53370444 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr19:53370422-53370432 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr19:53370426-53370436 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr19:53370430-53370440 | ATTAATTAAT | - | 6.02 | | POU6F1 | MA0628.1 | chr19:53370434-53370444 | ATTAATTAAT | - | 6.02 | | TFAP2A | MA0003.3 | chr19:53371654-53371665 | AGCCTCAGGCA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr19 | 53371445 | 53371755 | | chr19 | 53371155 | 53371399 |
| Enhancer Sequence | GGCTGGATGC AGTTACTCAT GCGCTGGGTG CAGTGACTCA TGCCTGTAAT CCCAGCAATC 60
TGGGAGGCCG AGGTGGGCAG ATCACCTGAG GTCAGAACTG TGAAACCCCT CCTGCAGGAA 120
CCCTCCACAT ACATGTAGTG AAGTCAACAC ACTCAGAGGC AGCCAGGGTG GCATTCTTGG 180
TAACGGTGAA AAACTGGGAA GGACTCACAC GTCTTCATTC AGAAAATGCT CCAAGGAGGA 240
TGAAAAACAG CAAACTATCT TGTTTCCTAC CTTGAAAATG TGGAACATTT TAACACTTGC 300
AGGATAAAAT ACCAGAACAA AACATTTATC ATGTCGAGCT CTTTGGCTCA CGCATGTAAT 360
CCCAGTACTT TGGGAGGCCA AGGAGGGAGG ATCACTTGAG GCCAGGAGTT TGAGACCAGC 420
CTGGCCAATA TGGAGAAACG CCATCTCTAC TAAAAATATA ACCATTAGCC AAGCATGATG 480
GCACATACCT GTAATGCAGC TACTCAGTTG GCCGAGGCTA GAAAATCATT TGAACCCATG 540
AAGCAGAGGT TGCAATGTGC TAGTAAGTTC CAGCCTGTTG ACAGGGTGAG ACACCTGTCT 600
CACAAAACAT ACAAAAAAAA AAAAAAAAAA AAAGAAAAGA AATGACTAAC AGTGTCAGAC 660
GGCTGAATTA TGATGTCACG ACTACAGTTA AATAACAGTC AGGCAATACG GCAATTCTAT 720
ATACACATAT TGCCCTTAGT TATCTAGTTC ACTATGCGTA AGATATAAAA CATAGAATGT 780
GTACTGGGAA AATTGATAAA CTGGGATCAG AGAAAACATA GTATAAAACA AATCGTATAA 840
TAAAAACATA AAAAAAGATG CAGGCTCCCT GGTCTGGATG TTCATATTGG CCAAAAGCCA 900
TGTTTGGATT TAATTAATTA ATTAATTAAT TAATTTATTT ATTTATGTAT TTATTTTTTG 960
AGATGGAGTC TCACTCTGTT GCCAGGCTGG AGTGCAGTGG CATGGTCTCG GCTCACTGCC 1020
ACCTCTGCCT CCTGGGTTCA AGTGATTCTC CTGCCTCAGC CTCCCAAGTA GCTGGGATTA 1080
CCGGTACGTG CCACCACCCC CAGCTAATAT TTGTATTTTT AGTATAGACG GGGTTTCACC 1140
ATGTTGGCCA GGCTGGTCTT GAACTCCTGA CCTCATGATC CACTTGCCTT GGCCTCCCAA 1200
AGTGCTGGGA TTACAGGCAT GAGCCACCGT GCCCAGCCCA TATTTGGATT TCTTATTCTC 1260
CAACAGGATG TTCCTGCAGA TGTGGCATTT GAGATAATTT GGTCATGGGT GTTGACTACT 1320
CATGAATAGG ACCAGTGCTT TTATTTTTAT TTTTTTTCTT TCTTTATTTT TGAGAAAGAG 1380
TTTCACTCTT GTTGCCCCTG CTAGAGTGCA GTGGCCTGAT CTTGGCTCAC AGAAACATCC 1440
GCCTCCTGGG TTCAAGTGAT TCTCCTGTAT CAGCCTCCCG TGTAGCTGGG ATTTCAGGCA 1500
TGTGCCACCA CACCCAGCTA ATTTTTGTAT TTGTAGTTGA GATGAGGTTT TACCATGTTG 1560
GCCAGGCTGG TCTCGAAGTC CTGACCTCAG GTGATCTGCC CGTCTCGGCC GCCCAAAGTA 1620
CTGGGATTAC AGGCTTGAGC CACCGCACCC GGCCATTTTT TTTGTTCAGT AGATTCAAGG 1680
ATTCAGCATG TTGGACTGAC TGGTCTCAAA CTCCTCACCT CAAGCAATCT ACCCCCATCA 1740
GCCTCCCAAA GTGCTGGGAT TAGAGGTGTG AGCCACCATG GCCAGCCAGT CTACGCCGTT 1800
TCTGACAGGA CAGTGAAATG ACGGAGACAG GAAAAGGAGC ATGTCATCAT CAACATTGCT 1860
GAAGGCTGAC AACTCTTATT ACACAAAGGC AGTTTACAGC CTGTCATATA AAAGCTGCAA 1920
TGTGTGAAGC CATCTAATAG CACTAACTTG TTTAAAAACC TGGAGGCATC CAGGCGCAGT 1980
GGCTCACGCT TGTAATCCCA ACACTTTGGA AGACCGCGGT GGGTGGATCA CCTGAGGTCG 2040
GGAGTTCGAG AGCAGTCTGA CTGACATGGA AAAACCCTGT CTCTACTTCA AATACAAAAT 2100
TAGCTGGGTG TGGTGGTACA TGCCTGTAAT CCCAGCTACT TGGGAGCCTC AGGCAGGAGA 2160
ATCGCTCGAA CCCCCGGGGC GGAGGTTGTG GTGAGCTCGG ATTGCGCCAC TGTAGTCCAG 2220
CCTGGGCAAG AAGAGCGAAA CTCTGTCAAA AAAAAAAAAA AATCTGGAGG CAAATTAACA 2280
TTATTTCTCA AATAAGTTCT CAAATAAGTA CAGCAGGCCC ACAGTGTTCA TGTACATGAC 2340
CCCAATTTGC ACATACAGTA AGTGAGGGAC AAACTTGATT CTTGGCCTGA AGGATCCCAC 2400
GACATGTTTC TAAGCAAAAT AGTCCACCAA GAAAGTACAG AAAACAACCA GTCACAAAAA 2460
ATGCTGCAAG GAGAACAGAA TGAAATACTA CAAGGGGGAT ACAAGCAAGG GCTGAGCTGG 2520
GACACAAGCG CTGAGCTGCG CTGCTGACAG TGGTTCTGAA GCCATCCCTC ATGGATCATG 2580
TGCTGAGTCA TGATGCCCTG CACACACTGA TTTAGGCAGC CTCCAATAAT TTTGTCCAGT 2640
GGATGAATAA GGTCTTGACT TACTCAGTGA 2670
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