| Tag | Content |
|---|
EnhancerAtlas ID | HS095-22652 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr4:78753900-78755380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr4:78754736-78754752 | CTTTGTTTACTCTATG | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 78754007 | 78754342 | | chr4 | 78754402 | 78754758 |
| Enhancer Sequence | TTTACATTTT CCTGTTTAAC CTTTATAACC ACCATATAAA GTATTATTAT TTTTCCCCAT 60
GATGCAAAAA ATTGTAGGTA CACAGGTTCA AATTTTTTAT CTTGTATCTA CATGTAGCTT 120
TAATGTGAAT CTCATGGCTG CAAGAACAGA CTGATACACA GATGTGTTGA TTTGTCATAG 180
GAGTGAAAAA TGAGAAACCT GAGGCTCAAA GATGCCAAAT AACTTTCTTC AGGAGAGCAT 240
GGATCCAAAC AGGTCTTTTT GATGTTTAAA TCCATGTGCT TAGCCACTAC AATATATTGC 300
CAAATGTAGT TTTTATTACT GAAAGCAGCT GTTCTCTTTC TATTCATACT TTTCTTACCT 360
TCTGATGTAG CTTCCCTTTG TAAATGGCTT TCCTTTTTTG TCTTTCTGGA ACAATTTTTT 420
TTTCTGGAAA CAGATAAGGC TGTTCCCCAC TTCCTCCCCA CCCCCCACCC CAGCCCCTTT 480
TAAAGTAGAG ATCTGTGCTA GATTTGGATC TGCTACAATT GATTCTAATT AATGTCCCTA 540
CCCTAAGGCT GTCTCTAAAA GAATGACTCA ATATAACTGA GCACATTTCA TTTTTAAAGG 600
AACTTGAGAG TGTTTAACTT GAACCAACAT GTCCAGGGAG TATACTCTTA CCTGTTCATT 660
GCCTTTTATT CCTCACCAGC CATTCACTTT TTAAATTACT AGATGGTTGC TTCCACTCCC 720
ACTGTTGTCA TCTAAAAATA TTATTTCAGT GATTATGAAC AATCTCCTCA TTAGTGGAGT 780
GTTTTTCTTC TCCATTACTA GAGTGGAAGT AATTTGAGGT CAGAGAATGT ATGCCACTTT 840
GTTTACTCTA TGATACTTCG TAATACTTAC ACATAGTAAA TTCACAGTAA CTGTCCATTG 900
AGTTCATGAA GCTGAGTGCA GTCTAATTTA GCACAATCCA TCGAGTTCAT GAAGCTGAGT 960
TCAGTCTAAT TTAGCACAAT AATTATAGGT AAATATGAAG ACTTCTTCAC TTAGATCGTT 1020
TGTGTTTTGT TTTCTACACC CATAAAATGA GCATAATTGT TCCTAAATCA GAGTTCTTGT 1080
GAAGATTCCA GGAGATGATA TTTGTGAGTG TTGTTAGATT ATATCAACAC ATGGCAGACA 1140
TTTAAAAAGA ATGGCTTTGG CCAGGCGCAG TGGCTCATGC CTGTAATCCC AGCACTTTGG 1200
GAGGCCAAGG CAGGTGGATC ACGAGGTCAG GAGTTCGAGA CCAGCCTGAC CAACATGGTG 1260
AAACCCCACC TCTACTAAAA ATACAAAAAT TAGCTGGGCT TGGTGGTGGG CACCTGTAAT 1320
CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATTGCTTGAA CCTGGGAGGT GGAGGTTGCA 1380
GTGAGCCGAG ATCACGTCAT TGCACTCCAG CCTGAGCGAC AGAGCAAGAC TCCATCTCAA 1440
AAAACAAAAC AAAACAAAAA AGAGTGGCTT CTCTTCCTCT 1480
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