| Tag | Content |
|---|
EnhancerAtlas ID | HS098-42880 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:113020060-113021510 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:113021010-113021029 | CTACCAGTAGATGGTGCCA | + | 6.11 | | FOXF2 | MA0030.1 | chr4:113021045-113021059 | TAAAGGTAAACAAA | + | 7.06 | | Foxa2 | MA0047.2 | chr4:113021365-113021377 | TGTTTACTTTGG | + | 6.74 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH04I112099 | chr4 | 113020941 | 113021070 | | GH04I112100 | chr4 | 113021181 | 113021270 |
|
Enhancer Sequence | TACAGAAGAA TGGCAGATCA GATGGCAAAA TATGAAACCA CAGCGATAGA CTTGGGCCAG 60
TTTACGCAGA GCTTTGTGTT CTGTGACACA TAATTTATCT TGTGGCTGTT GGTTCCCAAA 120
TGAAACAGCT GTACCAGAAA TCTTCTGAGG CATTTATTAA AATTCCCAGG GTCTCCAGTA 180
GAGCTACTGA ATCAAATCCC TTGAGGAGAG ATCTGAGTAT CTGGAGTTTT AAGAAGGGTT 240
CCCAGCACTC TGATAAGCAG CCAGTATAAC TACTGGTAGA CCAAGGGCTA GTCTGAGCCC 300
TCATCTAAGG GCTCTAAGCA TCTAAGTGCT TCAGAGAATG CAGCATCCGA GAGTTGCTGT 360
CAGGAATGAT CCAGCAAGGG GAGGAAATCA TAGTTGAGAG GTTCCATAGC CAGAAATAGG 420
TCAGCGCCAG AAAATTTCCA TAGAGAAAGG CATAGATGAC AAAGATGTGA GTTAAGTGAG 480
TGAGCTGGAC TACAAAAGCA GAAGGTATGG ACACAGAAGG CAGTTTCTGG AAATAAAGGC 540
AAAGTACAAC AGAGAGTTGT CCTATGTGAG ATGAGACAAA GATGGACTTC TGATGTGTAT 600
GAGGTGCTGC CAGAGATGGC TTAACAGCAG CCATCCTTAA TCCAGCTGAT GCCTTTCAGC 660
TGGAGTTGAA AAGGTATCCA GTTCAGTTAG CAGTTGAAAA GACAAAGCTA GGAAAACATC 720
AGGAAAAAAT ATCAGAGTTG GAGTTTGAAC ATTATGGTTC AATAGAAACT ACAGAAGTAG 780
ATGGCATTGC TGGAGAGGTA AAAACGGACT TTTAAGGGAC AGAGTAGATT TTTTAAAAGG 840
CATTGAATTG GCAAGAGGAG GAGGGAGTAA TGTGAACTGT CTTTTGTAAA TACATGGGAT 900
GTAGGATTGA ACCGTTTCCA TTATCTAAGC ATGTAGAACC GTTCTTTAAA CTACCAGTAG 960
ATGGTGCCAT AGTTTTGGAA AATAATAAAG GTAAACAAAG CCAATAATGT TACATGTAAA 1020
AACCTTGTCT TATGTTAACT TAAAAAAAAA TAGGATTTAT AAATGTAGAT TTAGAAAAGG 1080
AAAGACTTTG TTTCTTCTAA AGGCATTTAG AAAAATGCCT CCCGCAAGAC CAGAGACAGG 1140
CACTTCACAG GAGGAGTGCT TGGAGTGGGA GCTTTATGCT GAACAGGTTG GCTAAACGTA 1200
CATATTCAAC AGGTATAGGA GGAGCTATGA ATATTCATGA GGGTGGTCCT GACACATATT 1260
GGATGTTACA TGCTTATTGA ACAAACATGC ATGTAACATG ACCCATGTTT ACTTTGGGGT 1320
GGAGACTTAA CATTTAAATG TATTTACAAT TAGGCCCTAT AAATCAAAAG TTTCTTTCAG 1380
GGCAGGAAGG CATACAAGTG CACAATATCT GTAAACCGCC CAGAACCAGT CCATGGTCCA 1440
TGATCTTCTG 1450
|
