| Tag | Content |
|---|
EnhancerAtlas ID | HS136-20758 | Organism | Homo sapiens | Tissue/cell | Monocyte | Coordinate | chrX:13145470-13146880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF9 | MA0653.1 | chrX:13146809-13146824 | AGTTTCAGTTTTGGT | - | 6.46 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 13146302 | 13146550 | | chrX | 13146250 | 13146526 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH0XI013128 | chrX | 13146120 | 13146720 |
| Enhancer Sequence | CCTGGGCATT GTCTCTTCAC AGACAATCAG TCATCCACAG TAGAGAGAAG AGGGTAAATC 60
TTGGAATTAT TGGCTGACTC TTTGTGGGCA TCTAAACCTC CCTAAGCAGA ATGTCCGCAG 120
CTTTCACTGC ATATCCAGAG GGATTTAGTA CACACACAAA TCTCCAGGCC CTAGCCCATC 180
AGAGGTTAAC TGCACTTTGA GATCCTTGGA ATAGTGGTTC ATACTCTATC CATGATCTTT 240
ATGGGAAAGC ATTTATTTTA TTATTTCAAA AATGCACATT GAACACTACT GTGTACTAGG 300
TACTGTGCTA GGTATTAGGA ATTCAGCATT AGTAAGAGAA GCAGTCCCTA CTCTTGTGGA 360
GGTTATAATA TTGGAATGAG CTGGCTCAAG GAGAAAAGGG TCTGGCACAC AACCCTGAAT 420
GTGGTCAGTG TCTCCGATCA TTTTAGAAAA ATTAAACAAC AACAAAAACT TGTGCAAGTT 480
TCACAATGGA AGGATCCTTC CATGCATCCA TATAGATCCA AAACATTGCT AAGTGAGAGC 540
AAATATCATG AGAAACATGG AGTCTAAGAA AGCAAACAGA CAGAAAGCCA CATGAACCTT 600
TTGTATCGGG GAAAACTCAT ACAGGACTTT TGGTCTAAGT TTTTGAAAGA GGAGTGTTAA 660
GCTCAAATAC TTCCTCAGAA AACTTAAAGA AAACCTGAAG AATTCATTGA AGTACAAATT 720
GAACTAGAGA AGCCTTCAAT GATGATGTGA GGTGTTTTAT TTTGGTTTTA CCCCTTCATC 780
TTACAGTGCT AGAAAAGAAA AGCTGCTAGA TTTGGGGGAG TGGAAAGGTC CTCAAACAAC 840
CTGGTTCCTT CATCATTTTG ATCTCTTAGC CCTTGGTGAT TTTATTCTGC ATGGAGAATG 900
GCTATAGGAA AATGACATAG ACCATTATTT CTCTTGATTG AGTCATGTAA ACATGCTATT 960
GCAAAATATC AGAAGTTATG AGTCAGAAGT TATGCCAGAG ACTATTATAT AATAGGTTCC 1020
CCTATTTTTA GAAAATATGG TCAAAACCCA TTTTAAAAAC TAGATTTTGA TTTTTTGGCA 1080
TACTATGCCT TGGGGGATCT GTAGCAAGAC ACAAAGCCAT CATATCCCAC TCATTAACTG 1140
TTAAAGAAAC TACTGTCCAG AAAAAGAAAA TTGAGAGCAC TATGATTGTA TTTTAGATCA 1200
GAAAGACAAG CAATAGAACT AACATGGTTA TTTCAATAAA AACACCTAAG AAATAAGGAA 1260
AGTCTTATGT CACTAGATAA GAGAAGGCAG TTTTTCAACA GGGATCTATG GAAATAACAC 1320
CTTAAAAGAC AGATGAGAGA GTTTCAGTTT TGGTGAGAAT CATTTGACAT ACTTCGGAGT 1380
GGTTTGATTT TTTTCAAATA TTTCCAAAAT 1410
|
| |
|
|
|
