| Tag | Content |
|---|
EnhancerAtlas ID | HS127-32852 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chrX:19584210-19585540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chrX:19585248-19585259 | TGGGTGTGGCT | - | 6.14 | | NR2C2 | MA0504.1 | chrX:19584530-19584545 | AAAGGTCAAAGGTGA | + | 6.25 | | NR2F1 | MA0017.2 | chrX:19584529-19584542 | CAAAGGTCAAAGG | + | 7.22 | | Nr2f6 | MA0677.1 | chrX:19584531-19584545 | AAGGTCAAAGGTGA | + | 6.54 | | Rxra | MA0512.2 | chrX:19584531-19584545 | AAGGTCAAAGGTGA | + | 6.33 | | SP1 | MA0079.4 | chrX:19585246-19585261 | GGTGGGTGTGGCTTA | - | 6.01 |
|
| | 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 |
| GH0XI019566 | chrX | 19584199 | 19585491 |
|
Enhancer Sequence | ATTGCACTGT TGCACTCCAG CCTGGGTGAC AGAGCAAGAC TATCTCAAAA CAAAAATACC 60
ATTAACTTGA GAAGATATAG CCTTCTAGGA TTAATGTCTC TGTGGCAAAG AGAGAGAGAA 120
AACCAAACCT CAGTACTCTA TTTCTGGGCT CCCAAATATA TGCAACTGTG CTTAGTTTCC 180
ACAGCATGAA AAGCTTCTAT AGGTGAACCC GCCCCCCCAT CAATACCCCC AATATTTCCA 240
CACTAGCTCA TCAGACTGAA AAACATGTGA TTCATATTTT CATGATAGCG ATCATAGACA 300
TCTCCAGACC CAAAGAATGC AAAGGTCAAA GGTGAATGCT CTTAGCAAGC AAGACAGATT 360
ATCCTGTATA TTCTGGAGGA GGGAGAATAC CTCCCTTCCT ATTGACATGA GGGAGGTGAC 420
AAGACAGCCT CCTGAGGTCG CACATGACCT TCACCAACCA GCCACCCTGG CTTAAAACAG 480
GGCCCAAATA CGAAACTGCG GTGGTAGAAC CGGAACTTAG GCTCATTCTG ACAATCCCCT 540
TTCATTCACA GCCAATTACT GCTCTGCTCT GCTCTGCCTG CACTTTAAGC AGAACAAAAG 600
CTACAGCAGG CCAGAGTTTC TGTTATTGCA TCAGCCCAAG CTATCAGGTT ATGCTTCCTG 660
ACTGGGCTTC TCAAGGGCTG AGGATGTAAA CGAGCTTGTG GAAACAGGGG AAGTACTTTT 720
GGCATTAACA GTCACAGTCA CACATCCTAG CCCCAAGCCT GCATGAGATC AGACCAGAGA 780
CTGCAGGTCA GCAGTTGCAA AGATGCAACT CTATCAGCAG ATTCAGAGGA AAACAGCACC 840
CAAACAGAGG GACAGCAGCA GGAGAGCAGA ATGCTCATGT TGAGAGCTCT AGTGCTCTTA 900
CAAGGCCTGC CAACCATCGC ACATCTGTTT CTAAAGTGAG TGGCCCAAGC AGATGATGCT 960
GGAAAGCTAT CTTCCATGTC AAATCAATCC CTGATAGTGC TTGCCAGAGG TTAGGGAAGG 1020
GGGTGGGCTG GAGAAAGGTG GGTGTGGCTT AACAAGAGTA ACACAAGGGA TCTAGTGGTG 1080
ATGGAAATGT TCTATGTCTT GACTGGTGGT AGATACACAA ACCTACATGT ATGATAAAAT 1140
TGCAGGCTGG GTGCGGTAGC TCACAGCTGT AATCCCGGAA CTTTGGGAGG CTAAGGTGGG 1200
AGGATCGCTT GAGCCTAGGA GTTCGAGACT AGCCTGGGCA ACATAGTGCA ACCCCACCTT 1260
TACAAAAAAT ACAAAAATTA GTCAGGCATG GTGGCATGTA CCTGTGGTCC CAGCTACTCA 1320
GGACGCTGGG 1330
|
