| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00788 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:27396710-27398120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:27396717-27396732 | GGAGGGCAGGGGTCA | + | 6.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH01I027071 | chr1 | 27396941 | 27397090 | | GH01I027070 | chr1 | 27397346 | 27397995 |
| Enhancer Sequence | TGAGGGTGGA GGGCAGGGGT CAAGCACCCA GGGCCTCAGG TCATCTGTGT CCATCCCCTG 60
AGGCAGGCTC TGGGCAGCCC TCCCTGAGGA GGTAGCCCTG TCCCCAGGGC CCTGGATGGT 120
GAGGATGACC CAGCCTTCGT AACCCTGCCC TCACACACAG CGCTCACTCC AAAGCTTGCT 180
GGAATCATCT GAGGCTACCA GTGTCTACAG CACATCGAGC TACCCTTATG GAGCCTGGGA 240
CCAGCCCCAG GAAGCCAATC TCAGCTCAGG AGCCAGGATT TTAGTGCAAA GCTGCGCCCC 300
CTTCTGTAAA CCATGGTTCT CCTGAGAAAC AGCTCATGCC TTTGGTAAGC TCCTGGGCCC 360
TGGGGAGATG GAACACCTGA CTTGCGGCAC CTGGGGACCA TGTGACCAGA GCTGAGCACT 420
GTCTGACCTT GCCACAAAGT CAGGTGTGCC CAACGGTTTC TGTCATCAAG GGGAGAAAGT 480
ACACGTGGGT GAGGGCTGAG CGCAGGCATG TCCTGAAGCC CAGCTGAGCC TCTCAGCAGG 540
CAGCTCCTTC CCCAGAGTCC CTTCTCCAGC TTCCCAAAGC CCCTGCGTCC GCCCATACCT 600
TGGGCACAGG TCCCTAAGAC CAACTGAACA CTCGAGCATG AGCCAGGCAG ACAGCCTGGG 660
TGGATGCCAG CAGAAAGATT GGTGAAGACT GGATCTCCTG GGCAGAAGCG GTGACAGGCA 720
CATGGCGTCC AGTGTGAGGC TGGAGGCATC AGGGAGCACA GGGATGCAAG CCCCTCTACG 780
TTCTCCCTTG TCATGGCTGG GTGTGAGAAT GACCTTAGGC AATGGGGTGG GGCATGAATA 840
TTTTGAGCTT GTGCCAGCTG TGTGGTGGAG CGTGGGCCTG TACGGAGGCA CTGCACTCCC 900
ATCTCCCTCG GCTCCCAACT CCCTCCGTGG GAAGCTGAGT TCAGGCACTG CCCCTCCTGT 960
ATGGACAGGG AGCCACTGGT CCCAGCTTGC TGGTTGCCAG GCAACCCAGG ATGAGCCTTC 1020
GAGGTCATTC CTCAGACAAC TCTGAGCTCT CTCCACAGCC TGGGAACAGA TGGTTCCGCA 1080
GCAGCCAGCC CCAGCCTGAA ATGAGTTGCG GAGGCACTGC TGCCTGTCTC CACCAGCAAG 1140
AGGGAGGAGA GGCCCTTCCC GTGCCTGCAG CAGTCCAGGG TAGATGCAAG CAGAAAGACT 1200
GGTGAAGACT GGAGCTCCTG GGCAGAAGCA CTGACAGGCA CGTGGGGTCC TGTATGAAGA 1260
GCTGCACTTT GTGTGAAAGG AAAGGTGGCC CAAGGTCTGG CTCTACTTCA GCCGGGGCAG 1320
TGGCTGGTGG TCTTGCCGGG TGGGCCAGTC TTGGGAGGGG GTGATGGGGA AGTTGGTGAA 1380
ACAGAGGCAC TGGGTCAGCA ACTATGTGGT 1410
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