| Tag | Content |
|---|
EnhancerAtlas ID | HS073-15003 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chrX:44773010-44774320 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chrX:44773614-44773629 | TGTTAATAATTAACA | - | 7.04 | | HNF1A | MA0046.2 | chrX:44773614-44773629 | TGTTAATAATTAACA | + | 7.21 | | HNF1B | MA0153.2 | chrX:44773615-44773628 | GTTAATAATTAAC | - | 7.04 | | HNF1B | MA0153.2 | chrX:44773615-44773628 | GTTAATAATTAAC | + | 7.12 | | Nkx2-5(var.2) | MA0503.1 | chrX:44774026-44774037 | CTTGAGTGGTT | - | 6.32 |
|
| | 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 |
| GH0XI044913 | chrX | 44772974 | 44775800 |
|
Enhancer Sequence | GCACACACAC ATATATTCCA TATCAGCTGT CCTAGCTTGC TCCAGCATGC CTGGGCAGAA 60
CTAGACAAGT CCCAGCCCAT AGTGCATGCC ATTCCTTATT TGAAGATGCG TCCTTAACTA 120
TCCCTGGACA ACTTCCTTTT CTTTCTTTCT TCTGTTCCCC TTACCCAATT AAAAAAGTTT 180
TAAACCAGTA GCCAATTGGG TAAAGTGTAA AATGTGAGAT CCTATTTCAG CCAATGGAAA 240
CTGGACACAG CAGTAGGATC GATGTGTCAG GTTATAAATA ACCCTGTCTC CTTTGTTTGG 300
TGTGCTCTCC TGGCTGGACA GCTTATTTAG TAGCACCCTT TCTGCAGAAA GTAAAGCTCG 360
CCTTTCTGAG AGATCATTTG TTCCCGCATT AATTCTTTTT TTGTGACACC AAAAACTTTA 420
TTCCCAACAC TAGTTATGTT TTGGGGGAGT CAAAAGTTAC ATGTGAATTT TCAGCTGTGC 480
TGGGGGGGTC AGCACGCCTA TCTGCCTCGT TATTTAAGGG TCATTTGTAC TTACCTCATA 540
GGTTTCTGTG AATTAAATGA GCTAAGGCAT GTAAAGTGCA CCGTACTTAG CAGTGAGTAA 600
ATGTTGTTAA TAATTAACAA TTCTGATAAT CTACTTGGTG AACAAGAATA GGATATGTTA 660
GAATGATGTC TCATATATGT TAATGCAGAA GTTTTTTATG TCTCAGATAA GTTTTTTAGG 720
TAGATAAAGG AAATGAAGGA AATGATTCCA GGAAGAGCAC TGTGTCAGGA GTGAATCATA 780
AGAAAGATGT TACTATTAGG TTGTGGATTC TAGGTATTCT TTGGGATGTT TCTTTTTCAT 840
ATGTTCCCTG ACCCTATCCC TAGACTTTGC CACTTACCAG CTGTGAGACT GTGGATAGGC 900
TAAACTACTC ATCAAAGTAC CAGTTTTTGT AAGTTATTTA CTTTTGGAAA AGAACCAGAT 960
GTAATTCAAA GTTTTCTCTG TAATACCACC CTTCTTATTT ACATCTAGTA TACTTTCTTG 1020
AGTGGTTGGA CAAAGTGGGT GGCATTAGCA AAGCTAGCTT GGAACTGAGC ATAATACTGG 1080
ATACTCTTGT GAGAGTATGT CTGAAGTGAG AGCATTCTGT GGCCAAAAAG TCATACAGCC 1140
ACTGTCTTAC ACTATTTTCT TGGGTTAATT TTTGACCCAT AGTGGTAAAC CTAGTTATGA 1200
GTCTGTCCTG CTACATTTAC ATTCTGTGTT GATAGAAACA TTTGGAGCTG GCTAGGCTTT 1260
TCTAGAATCT AGACAACTGC TTTAGTCAGT TGTACATTGT GGATGTTTCC 1310
|
