| Tag | Content |
|---|
EnhancerAtlas ID | HS030-01897 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr1:174621360-174622830 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr1:174622220-174622236 | CTTTGTTTACACTGTG | - | 6 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 174621986 | 174622092 | | chr1 | 174622196 | 174622600 |
| Enhancer Sequence | TTCCCTTTGT GGGTATCCCT ACCTTTCTCT CTGGCTGCCC TTAACATTTT TTCCTTCATT 60
TCCACTGTGG TCATTCTGAC AATTATGTGT CTTGGAGCTC CATCCAGTTT TGTTCCCTTG 120
CTGGCAAGGA GTTGTGATCC TTTGGAGGAG AAGAGGTGTT CTGGTTTTTG GAATTTTCAG 180
CCTTTTTCCG CTGGTTTTTC CTCATCTTCA TGGATTTATC TATCTGTGGT CTTTGATGTT 240
GGTAACCTTT GGATGGCGTT TTTGCGTGGA TGTCCTTTTT GTTGATGTTG ATGCTGTTCC 300
TTTCTGTTTG TTAGTTTTCC TCTAACAGGC CCCTCTGCTA CAGGTCTGCT GGAGTTTGCT 360
GGAGGTCCAT TCCAGACCTT GTTTGCCTGC GTATCACCAG CATAGGCTTC AGAACAGCAA 420
GATTGCTTCC TGTTCCTTCC TCTGGAGGCT TTGTCCTAGA GAGGCACTCG CCAGATGCCA 480
GCCGGAGCTC TCCTATATGA GATGTCTGTC GACCCCTGCT GGGAGGTGTC CCCAGTCAGG 540
AGGCACAGGG GTCTGGAACC CACTTGAGGT GGCAGTCTGT CCCTTAGCAG AACTCAAGCA 600
CAGTGATGAG AGATCTGCTG CTCTCTTTAC AGCCGGCAGG CAGGAGTGTT TAAGTCTGCT 660
GAAGGTGTGC CCACAGCCTC CCCTTCCCCC AGGTGCTCTG TCCCAGGGAG ATGGGAGTTT 720
TATCTCTAAG GTCCTGACTG GGGCTGCTGC CTTTCTTTCA GAGAAGCCCT GCCTAGAGAG 780
GAGGAATCTA GAGAGGCTGT CTGGCTACAG TATCTTTTCT GAGCTGGGGT GGGCTCTGCC 840
CAGTTCGAAC TTCCCAGAGG CTTTGTTTAC ACTGTGAGGG GAAAACCGCC TACTCCAGCC 900
TCAGTAATGG TGGACGCCCC TCCCCCAACC AAGCTGGAGT AACCCAGGGC AACTTCAGAC 960
TGCTATGCTG GCAGTGAGAA TTTCAAGACA GCAGATCTTA GCTTGCTGGG CTCCATGGGG 1020
GTGGGATCTG CTGAGCTAGA CCACTTGGCT CCCTGGCTTC AGCCCCCTTT CCAGGGGAGT 1080
GTATGGTTCT GGCATTCCAG GTGCCACTGG GGTATTAAAA AAAACTCCTG CAGCTAGCTT 1140
GGTGTCTGCT CAAATGGCCA CCCAGTTTTG TGCTTGAAAC CCAGGGCCTT GGTGGTGTAG 1200
GCATCCGAGG GAATGTCCTG GTCTGTGGGT TGCAAAGACC ATGGGAAAAG TGTCATATCT 1260
GGGCCAGATT GCATTGTTCC TCATGGCTTC CCTTGGCTAG GGGAGGGAGT TCCCTGACCC 1320
CTTCACTTCC CTTGTGAGGT GACACCCCAC CCTGCTTCAG GTTGCCCCCG TACCCACTGT 1380
CTAACCAGTC TCAATGAGAT GAGCTGGTAC CTGTGTTGGA AACGCAGAAA TCACCCGCCT 1440
TCTGCGTTGA TCTAGCTGGG AGCTGCAGAC 1470
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