| Tag | Content |
|---|
EnhancerAtlas ID | HS048-25582 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr3:52187140-52188370 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr3:52187806-52187818 | TGCCTCAGGGCA | + | 6.18 | | ZNF263 | MA0528.1 | chr3:52187502-52187523 | GGAGGAGCAGCTGGGGGAGGG | + | 6.72 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAACTACTG AAATGTACAC TTTAAAAGGT GAATTCTGTG GTGTATGAAT AACTTAATAA 60
AGTTAAAACA CCAGAGAGAA TACTCCGGAG ACTCTCTCCA TCCAATAGCA GCTTGTGTCT 120
TAACACTTGA AGGGTTATAA TTCAGCCATC CAAACATCTC CCCCTACTCT AAGTATCAGA 180
AACCTCAAAG AAGCATTTTG GGTGCTCCAG GAAGCCCAAA GGCTCCTCCT GGGAAAGGAT 240
GTCCTTGGGG CACAGCAAAG CCACTGCCAC CCTACAGAGC AGTAACCAGA ACAAAGGCCC 300
TATGGCCTTG TGCCCAGCTC CACCCCTAAC GCACCTGTCA GAGTCTCCTT TCAACAACAG 360
AGGGAGGAGC AGCTGGGGGA GGGTCCCCAA CAGAGCCTTC TGCTCTCACC TAAGCTTCTT 420
GAAAGAACAT GCGTAAGAGA GTGTCCGCCC CTAGGCTCAG TGGGCAGAGG CAAGTTCAGG 480
TCCACCCCTG ACCAGTAGGT CCCATGGTAT CTCTCAACAC CGCCTCCCCT CTGTAGTTCC 540
CTGCATGTGG GCCTCATCTC CCTCAACAGT GGTTTATACA TGAGGGGACA GGAAGGGAGG 600
TAGAGTACCA GATTAGGAGT CAAAAGGTCT GTATCCTAGC CTGGAATCTC CGTCCATGTC 660
CTCAAGTGCC TCAGGGCATC ACAGGCTACC ACCCAGCCTC CCTGACTCTC CAATCAGCCA 720
GAGGGCCTTG CCCGTTCAAA GGAATCTCTC GAAATGAGGA CTTCTGGAGG AATGTGAACT 780
CAGAGAGGGC GGCTCCGCCC CGCTCACACT GCAGGCCCGG GCATCCCAGC GTCCTGCTGT 840
ACCTACCTGC TGGAGCAGGG TGTACCCTCA ACAAGACCCC ACGCAGCCAC CCACTGCTAA 900
GGACGTGGAG AATGGCTAGA GAGGCCCGAT ACCGGCCCCA GGTCACACAT GAGTCGGGAC 960
TTGGTCGTGT GTCCCTCGCT AGGATGCAAA CTATGGAGGC AGAGGCCTGT TTGTTCGCTC 1020
CAGAAACCCA GCGCAGGGCC TGGCACGCAG GAGGCGCTCA GAAAGTGCCC GACCCAGCGC 1080
CCCCTGCGCA GACAGTAAAC TGGACCTGAA GAGGACCACC CTGGAACCTG GCGCCCCGCC 1140
CGCCCCTCGC AGCCATCGCT CTGGCCATTA GGCGCCCAGT GTCCCAGCGG GGAGACTGAG 1200
GCCTGGGGAG TTGCTCTCGG CTGGGCTTAC 1230
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