| Tag | Content |
|---|
EnhancerAtlas ID | HS095-32482 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chrX:102892760-102894170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chrX:102893049-102893063 | CTGACTCATCTCCT | - | 6.29 | | RELA | MA0107.1 | chrX:102893709-102893719 | GGGAATTTCC | + | 6.02 |
|
| | 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 |
| GH0XI103637 | chrX | 102892375 | 102894535 |
|
Enhancer Sequence | TTCTGTCTAG ACTGCCCTTC CCTTCTCTGC TCAGCAAAAT TCTATTAAAT CATTAAAACT 60
CAACTAAAGT ACCACTTACT CTCAGATGAG TTAAGTGTTC TTTCCTGGTT CTCCTGAAGT 120
ATCCGGTGAC TTAGACTTCA TTATCATGTA CTAAAACTAT GTTTAAGCAT GTATATCCTT 180
TATAAGTTAA TGAACTGCTC AAAGACATTT GTGGCTTATT CATCAGCATA TACAGGACAA 240
AGGACAGAAC ACTCATTCAA TATATGTTTG TTGAACCAAA TATCAAGGAC TGACTCATCT 300
CCTCTGTTCC AACCTCTGTC ACCCATACCT CAGACTGAGG TTGTTATTGG CCCTTTAAAG 360
AGTACCTGAA GTGAAGACTA AGCTGTGACT GTGTTGGAGC ACAGCAGGGA AGGCCAAAAT 420
AGAATGAGTT ATGTGCTCTG AGCTTGTCTG GATTCTGGGA AATGCAGCAG CAGCCACAGT 480
CTGCAGGTGG TCCCCATTCA GGCCAAATGG TGTTCATCCC TCCTCAGCAT GGTGGGCACG 540
ATGGAATCAT AGCTTCCTAG AGCTAGAAGG GACCTCATTC ATGGTTCTAC CACAGCCCTC 600
GCCCCCACCA TTTAGGGAGA AAAATGATGC AAATAGAGGC AAGGAGAGGG GTAGGAGGCT 660
GCCACACCTC CAGAGCCTCC AGGGAGTGAA TGACAGCATA AGTCTTGCCC AGACCCAAGC 720
CTGGTACTGT CTCCCTTCAG CCCAGGTCTG GACCCACCTT CCCTGTCCTT GTACGTTTCC 780
AACAGCTTGA GTTGCTACCT GGCCTTTCCT CAGAGCCCCT TCCTTGTTAC TCTGAGCATA 840
TACAGTGTGT GTGTGTGTGT GTGTGTGTGT GTGTGTTTGG GCCCCAGTTA GGATGAGGCC 900
ACAGGCAGAA ACAGAAAAGA GGAGGCTCCT GTCATTGCTT TTCCTACTTG GGAATTTCCC 960
CTGGGGCAGG GGTAGGGGAG GAGCCCATGA GAGTCACAGG CTGGACAGGG CCTGCTGCAG 1020
TCAACAGGTC CAGGTCTGAG AGCAGGTACT GCCATTAGTG CCATTAGGAA AGAATGCAGA 1080
GGCAGCAGCC ACAGAGGGAA CGTCTGGGCT GGAGAGGGCA GAACTCCTCA AGTCCAGGCA 1140
GACAGGGCCT GCAAAGTGAA ACCAAGGGGA CTCGCAAAGA AGGAGGGTTC TGTTCCTGCC 1200
ACAGAAGTGC AGCCTCCCCA GCAACAGGAA TCCCTGGAGA AGAAACCCAC CCTGGGCTTT 1260
CTCAGATCCC CCAGAGAAAG GCCACACCCC CTGGATACTG TTGTCATGGC AGCAGCTGCC 1320
CAGTGCTAAC TCCCTTCTCC CTTTCCTGCA TGGCTGTCCT GCCTGCGTTC TGATACTTTC 1380
AGCTCCTGCT TCCTGAAAAG ATCTGTGCTG 1410
|
