| Tag | Content |
|---|
EnhancerAtlas ID | HS098-06480 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr10:28949830-28951240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr10:28950116-28950127 | ACAGGGTGTGG | - | 6.14 | | ZNF263 | MA0528.1 | chr10:28951051-28951072 | TCCCCTTCCTCTCCTTCCCTT | - | 6.13 | | ZNF263 | MA0528.1 | chr10:28951061-28951082 | CTCCTTCCCTTCTCCTCCCTC | - | 6.26 | | ZNF263 | MA0528.1 | chr10:28951047-28951068 | TCTCTCCCCTTCCTCTCCTTC | - | 6.47 | | ZNF263 | MA0528.1 | chr10:28951058-28951079 | CCTCTCCTTCCCTTCTCCTCC | - | 6.8 |
|
| | 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 |
| GH10I028660 | chr10 | 28949817 | 28950727 |
|
Enhancer Sequence | CATGGTGGCT TGCACCTGTA ATCCCAGTTA CTAGACAGGC TGAGGAAGGA GAATTGCTTG 60
AACCCAGGAG GCGGAGGTTG CAGTGAGCCA AAATCACGCC ACTGTACTCC AGCCTTGGCG 120
ACAGAGCAAA AGCAAGAGTT TAACTGACTT GAGGCTGGCC GTGTGAAAGA ACTGGAATTG 180
TCACTCAAAT CAGTCTCCCA GAAAACTGGG GTTAGGGTTT TTCAAGGATA GTATGGTGGG 240
CTGGAGACTA GGGAATGGAT GCTGCTAACT GGTTGGTGAT GAAATCACAG GGTGTGGAAA 300
AATGCTTCTT GTTCACTGAG TCTGCCTCTG GTTGATGGCC ACAGGACTGG TTGAGTCATG 360
AGTCACGATC CTGGGTGGGG CCAGTCGGTT GCCAGAATGC AAATATCTGA AAAACATCTC 420
AAAAGACCAA TCTGAGCTTC TACACCAATG GTGGTATCTA TAGGAGCAAC TGGGGAAGTC 480
ACAAATCTTG TGGCTTCTGG CCACAGAACT CCTGAGCAGT AAGGGATTAT AGAAACTATT 540
CCTACATTTT AGCAGAGTTC AGGACCCTCC CATAATTTTA ATCTCATCGC CTTTCATTAG 600
TTTTTGGTCC CTGAGCAAGG AAGGGGTTAC TTTGAGGGAG GGACCATTAT CATTCTTGCT 660
TCCAACTTAA ACTATAAACT AAATTCCTCC CATGGTTAAC TTGGCCTATG CCCAGGTGTG 720
AGCAAAGACA GCCAGCCTGT GAGGCTAGAG CAAGATGGAG TCAGCCATGC TACACCTCCC 780
TCACTATCGT CATCTTTCAA AGGCAGTTTC AGCCTGGAAG ATAAAATCAT CTCCAGGTCC 840
TTAGCGATTG GTGGGTCTCC CATTTATGGT CCTTGAAATG GAACCAGGTA TGGACCCCAG 900
GGGCCCTGGG GTGTCCCTTC CATGGAAGCC ATTTCCCTGA CTGGTGTGAG GGTCAGGAAT 960
TTCCCATAGA GCATTTTTCC ATAGGAGAAG GCCAAGCTCT GTGCAGAAGG ACCTTGCAAA 1020
TAAAATGAAG CATTGGAGAA AGCAGCTACT GACAGCTCCC TAGACAGGTT GCTTCCTGTA 1080
ACTGAAAGCT GAAATCCAAG AATGACCTAA AACTCATTCC CAGAATTCCT TACTTTAGGC 1140
TCATAGAAAC TGAGACAAGT TTGGGAGTGG TAGTTATTTA ATCAACTCAA AAACAGCCCA 1200
TATTTTCAGC TATAAAGTCT CTCCCCTTCC TCTCCTTCCC TTCTCCTCCC TCTCTTAACA 1260
ATTTCTTGCC ACATCCTGTT CAAGGAGAAA CAAACCACTA TTTGCCAGTG ATGATCCCTT 1320
CATAGCTTCC CAGCCTTTGA GATGGAGGGT GGTGTCCTGA ACTCAGAGCT TCGGTGCAGT 1380
TGGTGTGACC TTGAGGAAGC CATTTAACCT 1410
|
