| Tag | Content |
|---|
EnhancerAtlas ID | HS076-58127 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chrX:71238000-71239440 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:71238602-71238621 | TGCCCGGCAGAGGGCGCTG | + | 6.11 | | FOSL1 | MA0477.1 | chrX:71238495-71238506 | GATGAGTCACC | - | 6.32 | | JUND | MA0491.1 | chrX:71238495-71238506 | GATGAGTCACC | - | 6.62 |
|
| | 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 |
| GH0XI072018 | chrX | 71238051 | 71240910 |
|
Enhancer Sequence | TTCAAGGACC TCTATGAGGT GGTCCAACCT ACCCTTCCTT TGCTTGTGTG GGGGTGAGGA 60
CCTGGGAGGT TAGGGGGACC ATGCAGCTTG ATGCTATGGA AAGCACACCT CGAGCTCTGG 120
AATCAGAGGT TACTGGTTAA TCTAGGCCCT CCCCTGCTTC TTATCTGCTT GACCCCGGCC 180
CTCGCCTCAC CGTTCCCCCG CCCAGTTTCC CTCTTGTTAA GGTGGTGTGA TAAAAACGAC 240
CCCTATCCCG GGTTAGAGGT GAAAACTCAA CGCGACAAGT GGAGGAGAGC GGGCTTTTAG 300
CGCCAGAAGC TTCCATGATG CCCAGGTCCG CGGGCAGGGC GAGGGCACGG GCCGGGGAAG 360
CAAGCGTTGC CGCGCCGCTA CCGTCGGGGG CCGGCCCCCG GGCTGCTTTT CGTGCGCGGA 420
GCAGCTCGGC CAGTCACCAG GCGCGTGCGG AGGCGGCGAG CCTGCGAGGG CGGCCGGTGC 480
GGGCGCAGCC GGCGCGATGA GTCACCATCC CTCAGCACCT CCGGAACACG AGGCTGCTTG 540
GAAGCAGCCG GGCCCCCGCC CGCCCTCCTC CCCCGCCCCG CGGAGTGGCG GCGCCAGCCC 600
GATGCCCGGC AGAGGGCGCT GCAGTGCGGC TGCGGGGCCA CCGGCCCGCG CTGCTCTGGC 660
TGCCAAAGGC CGGCGCTGCC TTTGGCTCAG AGGGAAAGAT CGGGGCCCAG GGATGGGGTG 720
CGTGAGGAAT GAATGTTTCT GCAGTGCCAG AGGTGGCTCT GTTTTTGATC CAGAAACGAA 780
ATGGACTTCA AGATTCAGAC ACTGGGCAGA GTGATGGGGC CGACACGGCC CCTACTGGAG 840
AGTGTCCAGT CTTGATCGCC CCAAGCTTTT GAGCAGGGAT GTCCTGTCCG AGGCTGGTGT 900
CGTCCCCACT CTCGCCAGAG AGGATCTGTG ATAGGATGAG TCTCGCCTTT CCAAAATGAA 960
TCTGCCTAAG GACCCAGTCC TTGATCTCCT CTGTGACCTC TTTCACCTGA GGTGATGGAG 1020
GTTACGAAGA TTGGAGCTGT CTGCAGTGGA GCGCAGGAGA AAGTGCACAA GCTTTCGGGT 1080
GACCAGGGTT TCAGTGCCAG CTCCATCATG AGATTGCTGT GTGACCTTGG TCATTTCATT 1140
ATTCATTCAT TCATTCAGAA AACACTCACT GTGTCACAAG GCACTCACGG TGAAGGGAAG 1200
AGAAGGAGGC CAAGCCTGTG GAGACAATTG CCCTGACCAT AAAATAGCTT AGGCCAGGTA 1260
CAGAAACCCG ACACGTAGGT AAACACTGGC TGAATGAACA AATGCGATGA TTTAGTCACC 1320
ACACACTAGG GCAGAGATTT TTGGTCACTT ATGCTCCCGA GTACATGGAA CAGTGCCTGA 1380
CACACAGTGG GTGCTCAGTA ATTTGTCGAA TGAATGACAG AGGAATGTAC TGAGTGTTCT 1440
|
