| Tag | Content |
|---|
EnhancerAtlas ID | HS062-03059 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr11:72141600-72142970 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:72142199-72142218 | TGCCACCACCTTGTGGCCA | - | 6.67 | | Gata1 | MA0035.3 | chr11:72142538-72142549 | TCCTTATCTGT | + | 6.14 | | USF1 | MA0093.2 | chr11:72141951-72141962 | ACCACGTGACC | + | 6.32 | | USF2 | MA0526.2 | chr11:72141949-72141965 | TCACCACGTGACCATG | - | 6.07 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 72141800 | 72142158 | | chr11 | 72141871 | 72142478 |
| Enhancer Sequence | ACACCTTTCT ACTACAGAGC CCAAACTCTT CACTCCTCTC ATCATAGAGG GAATGCAGGT 60
CAACTGCTAG CACCACGTCT TGCCTATGGT AAATAATGTG CTCTTCATAA TCTATGAAGC 120
TCTGCATATG CTTTATGTTC CTATAAGAGT TATTACTAAA GATTCCCTGA TCTTGTCCAC 180
TTTCTCCCTC AACTCCAGTT CTTCAACCCA GTTCTGAATC TTGATGTCAA GTCATAAACC 240
CAAAAGGAAA GGTAGAATGG AGAGGAGCAA GCAGGGTGTA GGCCTCTCTG AGGATGGAGA 300
GGTCTCAACT AGGAGTCTTT GAGATCTAGC TCCATTCCAC TCCCACTACT CACCACGTGA 360
CCATGACAGC TCCTCTCTCT CTCAACCACA GCTTTCCTGA CTGTAAAACA TAGACAAAAC 420
TCCTTGCCCT GCCAGCTTCA CAAGGATGTC AAGGAGATGA AATGACAGTT GAGACGTCTG 480
CAAACTCCCC AGTGCTGAGC CCAGGGAAGG GAGACCCAAA GCAGAGGAGA CACTAAGCCT 540
AGGAGAAAAG CAACGCTAGC TAAGTGCGTC TGGCCTGGTC TGGGCAGCCT GCAGGCTGTT 600
GCCACCACCT TGTGGCCATA AAGAAAATTG GACTGACTCA GAAAAACTCA AAAGTCAACA 660
GGAGAGGCAC AATCTTTTCA AATAGCTCAA TACCAGGTAC ATGGAGCCCT CTGTGCCCAG 720
CCTGGTTCTG AGCTACACTG CTGGGCAGTG GGCGGATTCA TAGCCAGCCC TGACTCAGGG 780
AACTCTCAGT CCAGCCAAAA GACTCACTCA TGAGCAAATG CACTGGAGTA GAGTGAAAGA 840
GCAGGATCTG GAGACAGTCA GACCTGGGGT CTAGCCCAGC TCTGTCGCTT ATTTGCTGTA 900
TAACCTAGCC CACCTATCTA ACCTCCTGAG CCTTAGTTTC CTTATCTGTA CAATACACCT 960
TATCATGCAT ATGAAAGCCA GTCCTGTGGT TCAGACATTG ATGCCTCCTG GCCTAGATTC 1020
CAGGGACAGG TCCTTTCTAC TTACCTTACC GGATGTACCT AAAGCACATA CCCAAGCATG 1080
GCTCAGACAG CCACCAGCTG GGAGGGGATC AAGCCTTCCT TAGAGATGGC TATATCCACT 1140
CTCCCTTCAC TCTGCAGAAA AAAATGTGGC TTCTACAAGG TTACAGAGTG AGGAATGAGC 1200
TAAGAACCAG GGCCTCCTGG CTTCTAAAAG GGTTCAGTTT CTACCACACT GCACTGAGGG 1260
TCAAAACTCT AAGTCAGGGG ACAGGGTAGC TGGCAAGTCA GTTCCAGCAG GAACTGGTCA 1320
CGGCTTTGAC CATTATCTAT TTTGGTAAAT AGACCCTGGT ATTCTTGCTG 1370
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