| Tag | Content |
|---|
EnhancerAtlas ID | HS147-44339 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chrX:117125460-117126780 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PROP1 | MA0715.1 | chrX:117126700-117126711 | TAATTTGATTA | - | 6.02 | | ZNF263 | MA0528.1 | chrX:117125727-117125748 | GGAGGTGGAGAAGAAAGGAAA | + | 6.21 | | ZNF263 | MA0528.1 | chrX:117125724-117125745 | GAGGGAGGTGGAGAAGAAAGG | + | 6.22 | | ZNF263 | MA0528.1 | chrX:117125720-117125741 | GGGGGAGGGAGGTGGAGAAGA | + | 7.12 |
|
| | 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 |
| GH0XI117989 | chrX | 117123715 | 117126505 |
|
Enhancer Sequence | TTTATTCAAA AACTTTCCAT GACTCCTTAT TTCTATGGAT GTATTTGTAG ACTCCACTTT 60
CAAGGTCCCC TCAACCCCCA GCCCCACCTT ATCTATTCAA CCCTATTTCC CATTACAGGT 120
AATCCCAGAT TTGCACACAA CTAAAAAACA CAGTACCACC ATACCCAGAA CTGCTACAGA 180
AGTTATTCTT AAAAAGTAAT AATAATAAAC AACTTGCAGC CTATAGTAAA CCTGTGAAGA 240
GGAATACACA AGAACAATTT GGGGGAGGGA GGTGGAGAAG AAAGGAAAAT TAGGCAAAGC 300
TCTTGGCCAA AGCTTTCCTT ATCTCAAAAT ATCTTCTCCT ACAGTGAAAC TCTCTCTCTC 360
TCTCTCTCTC TCTCTCTCTC TCTCTCTCTC TCTCTCTGTA ACCCTCACCC CCCTCCCACA 420
TTGTTTGCTC TGTACCAGTG CCAGAAATTC CAGCAATTAC AGGTTCATTT GAGCTAACAA 480
GAAGGCTGTT AAAATTAAAG TAAGTACAGC TGCCAGGATG AGGTGGCTAT CAGTTATTCA 540
CACATTGGCA TGAATGAGTT GAGTCAAGTT TCTTCAAATA GCAAAGAGCT GTTGCCCTGA 600
GGGAATGAGG CAGGCTGGAG GTGAGAGAGA GCCTTTTAGA GCCCTAGCAA CTTTGGATGG 660
GGTTCTGTTT CAAGGAAGTT AGCAGCATGG GGTGCCTTGA GGGATAGAGA AACTTTCTCT 720
TAGAGAAACT GAGATGTAAA AAAAAAAAAA AAGGTGCAGA AAGGGTCATA GGAGAACAAC 780
AAATCTCAAT TTCTCTATCA CTCTGTCTTC TAGCCCAGAA TCCATCGCAC CTTTCCTGAC 840
TCTCTGCTCC CAGGCTCTGG AGCACTGTCC CTGGGATAGT TCACTACTAA GTAGGTTAAA 900
TACAATATTT TGAGCTGGCT AGAAACCATG TATATTATGT GTCATGTCCA AACAAATGGT 960
TTGTAAATAA ATCTTTAGAA CACACCCTGT TTATAGGTTA TGATCTACTT GTAGTTTTCA 1020
ACATATACCT TCCCCCCATC AACACACATA CACACACCCT AATTAGACTG GTCTCTTCTC 1080
TGTTTTGCTA AGGCTGGGCT TTTTTTTTTT CCTTTTTTTC TGTCACCACC CATTCAACTC 1140
ATAAAACATC CCTTTTGCAT AGTAGATTGT GGCTGCCTCT CTGTTCACAC AAGTTCTGCC 1200
CATTCTTAAG TTCTAAATCA AGCTCTACCT TTTTGAAGTA TAATTTGATT ACCCCCAGCA 1260
CTCCCCTTTT CTTTCTAAAC TCTTTCAGCA GTTACTATAC AATGTTCATA GTTATTTATT 1320
|
