| Tag | Content |
|---|
EnhancerAtlas ID | HS191-03953 | Organism | Homo sapiens | Tissue/cell | Trophoblast | Coordinate | chr1:245784890-245786320 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:245785151-245785161 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr1:245785151-245785161 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr1:245785151-245785161 | ATTTTCCATT | + | 6.02 | | Nfe2l2 | MA0150.2 | chr1:245785054-245785069 | TGCTGACTCACCTTG | - | 6.08 | | RUNX1 | MA0002.2 | chr1:245786277-245786288 | GTCTGTGGTTT | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCCTTTAAC CCTGCAGTCT TGACCTCAAA ATCTGGAAAG TCAGTGAGGA ACCTGCTTCT 60
TACCTGCTAT TAATTATCAC CTATTGTGTT CATTTGCTGT GTAACTACAC TTTCTCCCCA 120
GCCGCCGGAA GTGATGGAAA TTCTTGATAA TAGCAAGTGG CCTGTGCTGA CTCACCTTGT 180
ACTATTTCAA GTTAAGCACC ATGTGTGAAA TTCACAATTC TGTGCCTACG GCAACTCCAA 240
TAGGCACGGA GCAGAGAGTA GATTTTCCAT TGTCTAAATG TGACTCTTAC TTTGAGTCAC 300
GCAGGTATAA TTATAGGTAT TTTATATTAT CATCCTCAGC ACAGTCTAAA CTGTGCCTTT 360
TGTTCTTGTG TTCTGTTTTA CTACATGTAC ATTATCCATT TTATTCCATT ACATCAAATG 420
GACTGTTAGA GTCAGAATTG GTCTCTGTCT TTGCCCTTTA ATCTGTGGTG CATGTGGAAT 480
ATCTGAGCTT CTCCTGTCTA TATAATTAGG CTGCAAAACA GATGATATTT TGCTTTAAAA 540
ATAACTATTT CCATAGCACG CTGCTGTGAC CCAAGCTTGC AGGGTACAAA ATAGCATAAA 600
ACAGAAGTGA CACATTATAT CTTCCCCTTA AAGGGGTTTT ACTGGGAATA GTTGAAGAGA 660
AACAAAATAT AACATCCTTA ATGTAAAAAG TTCTTTGCCA TAGACGTGCC AGTAGCTGGA 720
GAGCTGGAAT TGCAATGCTT TCTTTAAGTA TTTCTCACCT TTTTTTCTCA GTACTAGATA 780
TGGAATTTGA GGATAGGAAG GGGTGGAGGC AGATTAGCCT TAGGACAGTG GTTGCCGAAT 840
ATTTTCATCC TACAGCATGA GCAGTGCTGC ATCAGCCTTG TCCTTCGGGC TCTTCTGCAG 900
ACGCGTGGAT GCCTAGATCC CTCCCACGCA CCCCGAGTGC CACCTGCAAT GGTCCAGACA 960
CACGCGGGTC CCACACGCTC TGCTCGCTTT TTGTACCAAC ACCTTTCAAT CTTGCCCCAA 1020
ATTACTTGGC CTCCACAACA GCTTTGGGAA GTTTCCATCT CTGCCTTTGC CATTTTCCTT 1080
CTGTGCAGAG TAGGGAAAGG CAGAGGGAAG AGTTGCTGTC CTGGCAGTAA CAGGAGGCAG 1140
GCCAGGTATG AGGCTGTAAG CTGGGCCGCC TGGAAAGATA GGGATCCAGA GGCCTGGAGG 1200
AGCAGCATTC CGCTGCTGCC TGGGATTGAG GCGGGGGGAA GGGAGACAGC CAAGGAGTGG 1260
GTGATGTACC CAGAGACACG CCTCTCTGGA AGAGTGGGGC CTGGGGCAAA AAGGCGGCCT 1320
TCTCCGGCTG CTTCGTGGAG CTGATGGAGG CCGCAGGATG TAGTTGAGAG CTCAGGTCTT 1380
GCAGTCAGTC TGTGGTTTGA ATCCTAGCTC TACTACTGGC TGCAGGATCG 1430
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