| Tag | Content |
|---|
EnhancerAtlas ID | HS170-01139 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr14:94000030-94001350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr14:94001209-94001220 | TTTTATTGCTT | - | 6.32 | | STAT1 | MA0137.3 | chr14:94000557-94000568 | TTTCCTAGAAA | - | 6.14 | | Stat4 | MA0518.1 | chr14:94000554-94000568 | TTGTTTCCTAGAAA | - | 6.09 | | TCF7L2 | MA0523.1 | chr14:94000996-94001010 | TTCCTTTGATCTTT | - | 8.42 |
|
| | 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 |
| GH14I093533 | chr14 | 93999607 | 94000699 |
|
Enhancer Sequence | AGCATCATTT CTGTAGCATT CAACAGGTCA AAGCAAGTTC CAAGGCCGGC CCAGATTCAA 60
AGAGTGGAGA AATAGGATCT TTGTGGTTAT TGAAGGATTG GCAAGAATTT TATGGTCACA 120
TTTAATCTAC CACAATCTGT CCTTTGGACA TAATTATTTA CCTTCTTTCC ATATGCAAAA 180
TATGCTCACC ATTTTATATG ACCTCCACAA GTCTTATTCA TTTATGGCTT CAGGCTTAAA 240
GTCTAGTATC TTGTGATCTG CATGTGATAT GTCACTGATT AAACTTCTTG GTAACTGATT 300
CTCTTGATTC AGAGTCCTGT GAACTAAGAA GGAAAGTTAT CTTCCCTCTC TGCACCCAAG 360
ACACAATGTT GAGACAGGGA CAGGATCATA GCAATAAGCT TCTGTTCAAA AAGAGGAAGG 420
GAAAGCAGAT AGCAGTCATT GGTCTATAGC AGCTCCAGCC ATAAACACAT CAACAGTTCC 480
TCTGTCTCCA GGAATAGCAT ACATGCCTTG ATTATGATCT GGTTTTGTTT CCTAGAAATA 540
GTTCCCTAAT CTGTTCTTGT CCTCCTGAGC TCTTGGCTCC ACTCTCTGAG ACATCTTTTC 600
TTTTCAATAA GAAATGGTCC ATGTTGCAGC TGAGTAACTT TCTCAATCTG CTTCGTGCAT 660
GTAGGAGTTA GGGTCCCATA TATCTCTTTT CATTTAGAAC TGCGTCTCTT TAGTTTTAGC 720
TGGTGGTGCT TTTGCTAGTA TGACTTTCTT AAAAACTTTG TGGATTTTTA GTGAATCTCA 780
TTGGGGTCCT GAGCCCCCAA AGCCACATCT ATAATGATTT TTGAGGCAGT CCTTCCTATA 840
TTTTGGGCGT TTCAGTGTGC CCTTAAAATT ATTAGAAGCC CTGTTATAGC TGAGAGCCTC 900
AATTAGACAT CGCCTTATAA CTTTCTGAAG CCTTAACAAA GGATCTTAGA GTCATAGACC 960
ATATTCTTCC TTTGATCTTT ATCCTGAGGC CATTCTTACT TTGAGAATCG TTTCTAAGCT 1020
TGTGGGACCA GGATTTCAAA CAGTTCTATT TTCTAAATCA GCATGTTTTG GCTCTGGGGA 1080
CATACGTAAC ATATTTGACA CCCAGGGTAG ATCATTTTTT AACACTTCCC TCTTTATATG 1140
ACAAACTTAT TTTTAGTAAC AAGCTTCAAA TTAGCACATT TTTATTGCTT ATCCTTTAAT 1200
AAACATTGTG TTTTACACAG ACATTAATTT GGAGAATTTC CATTAAGTTC ATAACAGTTC 1260
AGAATTGTAT GAGCTTGCCC TGGGTAGTTT GTATTCTACC TCTTTGTACT GCATATTCCC 1320
|
