| Tag | Content |
|---|
EnhancerAtlas ID | HS037-42632 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chrX:119273500-119274930 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chrX:119274454-119274465 | ATTGCATAATA | + | 6.02 | | NFAT5 | MA0606.1 | chrX:119274199-119274209 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chrX:119274199-119274209 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chrX:119274199-119274209 | ATTTTCCATT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chrX | 119274200 | 119274816 | | chrX | 119274242 | 119274656 | | chrX | 119274691 | 119274772 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI120140 | chrX | 119274261 | 119274410 |
|
Enhancer Sequence | TCTATTATGT AAATACATGT AAAGCCCTGA TAAATTTCCC CAAATGTCAT TGTTACAAAC 60
CTATTTATAT CTTTACTACA GAGCATATCG TGGGAAAATT TTTTATTTGA AATCACACGG 120
TTAAGAGTTC AGAATTGGTT AGAAGAGTAG GGAATGGCTT ACGCTAATAT ATCTACAATG 180
ACGTATTTGT GTTCCTGTAG TGTTAAGGAT AGGAAGACAA TGGATATTCA ACAGCAGCAA 240
CAATAATATC AACAATTAAT CTAAAGAAAC TTACAAGAAA ATATGACTAA ATATTTACCC 300
ACTTTTGGCA TTTGAGTTTT GCTTTCAATT ATTTAAACTG GATTTCCTGA AGTATTTAAT 360
TTGAAATGTG AATATCTGCT CTCTTCAAGT GATACCTTTT TCCTTTGCTG TTTTTAATGT 420
GTTTTCTGTA GCTGTAATAA ACCATAAACA GGTGTCTGAC AGCTTTTCTG AGTCCAGAAG 480
CACAGAATGC TCTATGAAAG ACCATGATCC ATTCTCTCTC CTATCAACAT GTTTTTGTTT 540
GTTCTGTACC CCATTTGTTT TGTCTAGGAG CAAACACACA GAGATCTTAA GCCTATTAAA 600
GTTGTGTTTT GGCTTAGTTT CGGTACACAT ATCCTTTTAA TACAGCAGTT ATTAAAAATT 660
ATTTTAGGCA ATTAGAAAGG GTAAAGAGTT CTTGGTGGAA TTTTCCATTA ATAAAAAGCA 720
GCCCCCAAAC CATTTCTTTT CTAACAGAAA GCAGCCTGAA ACTTCAAGCT GCAAGCATAG 780
CTATGCAAGC TAGCTTTCAT ATGTAAATGC CATCAGCTGT ACCTGGAAGC CAGGTACATT 840
CAATATGGCG ATTCTCGCTC CCTTTTCTTT GTGGCCACGT GTGCGGGTGT CATGGCACTA 900
GCCAGGTAAA GTCACATGTG CAGGTGTCAT GGTGACAGTC AGATAGAAGC CATAATTGCA 960
TAATAAAAGA TTAGGGTTGG AGGGCCAGTC TTTTCATGGA CTGTGTAAAT GGAGCACCTG 1020
GTCAAACCAA TCCCCTGGGC TCTATGTAAA TCAATCACCG CCTCCTCAAG CCTTTGTACA 1080
AAATTGATCA CGTTCTGCAC CTAACCCAGA AACCCTCTCT CAGGTGACCC GCTTTCTCAG 1140
CATGAGGAAG CTTATTCTAT CTCTCTTCCT TTTTGTCTGT TAAACTTTCT GCTCCTTAAC 1200
CCACTCCACG TGTGTGTCCA TGTTGTTAAT CATCGGCGCG AGACAACTAA CTACAGGTAT 1260
TGCCCCAGAG GAAGTGGTTT CACTTTGAAT GGTTTGGCAC TATTGTCAAA TATCATACTT 1320
GTTATAAGTC TTTGCAGATT TTCTATTTAT TCTTGAGTCA GTTTTGGTAG TTTGTGTGTT 1380
TGTAGGAATT GTTTTTCAAT GTATTAGGGC ATCTAATTTG TTGAAATACA 1430
|
