| Tag | Content |
|---|
EnhancerAtlas ID | HS062-04543 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr13:43876890-43878350 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr13:43876921-43876937 | CTTTAAGTAAATAATC | + | 6.15 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH13I043300 | chr13 | 43874891 | 43878109 |
| Enhancer Sequence | CCATGGGAAC AGATAATGCC ATGCTTAACT TCTTTAAGTA AATAATCTGG AGAAAGCCTT 60
GAAATCTCTT TTACCAGCCT GAGCCAGCCT CAGAAAAATA GTTAGCAATA TATGAAAAAT 120
GTAAGTTGTT TTGGGTTATG TCCCAGTAAG CTGACAGTCT GTTAATATCT TTTTCATGCT 180
CAGGCAAGAT GTAACTAAAT AATAAAACAT TTTAACATAT CGTTTCTAAC AATATCTGTG 240
TTTCTCCAGA ACTCTTAGTC TTTGTGTGTT TGGGGAACTC TGTGTTTAAC ATTCCCCCTC 300
CACTTTGCCA GATGTCCTCC TGAAATGCTG GAAGGACGCT GCTGAACTGT AGATTTCCTT 360
CCCACATGCA AAGAAAGTCT TTTTCAAGAA TTTCATTGGC TGCTACCCAG GAAGGCAGTT 420
GTACCGATAG CCCCTGAACA CAGGAGGGCA GAGGCAGGCT GGCCTGGCAA ATGTCACCAC 480
AATATCTGTG TGCCTTCAAC GGCTGCCTCC TCAGCCACGA TCCTGCCTCC TGCTCCACTA 540
GGAAAGGGAG CTGTAGTTAT GGCCCAGTGA CAGGGACTCT CTCCAGCTTC TATCTGCTTC 600
TCTGCATTCT GAATCTTCTT GTGAGGTGCC TTGAGGCCTT TAGAAGCTAT TCTGTGGCAG 660
AGACATTATC ACGCTGTGTA CTCAAACTCA TGCTTCTCTT TGTATAGAGC AGTGTTGCTC 720
CTGAGAGGTG ACTGCCCTAG AGGGTGCCAT GTGAGCAGTC TCATCAATGG AGTGTGAGGG 780
GGAGTGAGGA TGCCTTCTGC ACAGTCCCTC AGTCTCTGCC TGCTGCTGGA ATAGGCTTGG 840
GTCTCTGAGT CACCACATGG AGGAAAGGTG CCCACAGGCC CAGAATATCT GCCTTGGACT 900
GTTGTGTGCC CAAAAAGTAA CACTTTTTTT TTTGGTTAGG CCATCTTTAT ACAGCAGCTG 960
GTGTTACTCT AACCCAGTGT TCTCCAAACA TTGGCCTGCA TTACAAGCTC CTGGCGGGCA 1020
TATTAAAACA CACTTTTCTG GGCCCTACCC TCAGTTTCCA GTTCAGTTTG TCTGGGAGGA 1080
AGCCCAAGAA TTAGCATTCT TCCAAGTCCC CCAGGTGGTG CTGATGCTGC TGGTGCAGAG 1140
ACCACACTTT GAGAGCCACT GCTCAGACCG CTGCTCATTC TATCCCGATT CCTAAACTGG 1200
GGTTGTGGTT GGCTTGTTTG GAGAAATGCT TCTGAAAGAA CCACATGCTT GGCTTGTCAT 1260
TCTGGTTTTA TTCCTTGATC TCCTTTTGTA TGAGCCCCGA CTCCATGTTC TGCACCTGGG 1320
AAGGCAGCCC TGTTGCATCC CTGTGCCCAG GTCCCATGAG CTCAGCTTGC CCCGTGCCCT 1380
GGCTATCTCC TATGGAAGAT TTGGGCAAAA GGCACAGTCA CTATTCTGCT TTCTTCAAAT 1440
AACAGTAGCA GTAATGGGAA 1460
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