| Tag | Content |
|---|
EnhancerAtlas ID | HS138-00645 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr1:32297110-32298130 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:32297742-32297760 | GATTCCTTCCTGCCTGCC | - | 6.02 | | HNF4G | MA0484.1 | chr1:32297152-32297167 | TGAACTTTGAACCTT | - | 7.37 | | Hnf4a | MA0114.3 | chr1:32297150-32297166 | ATTGAACTTTGAACCT | - | 7.05 | | Rxra | MA0512.2 | chr1:32297152-32297166 | TGAACTTTGAACCT | - | 6.55 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGGGCCTCT GGTCCTGGGG ATCTCAGAGC TGCTGGACAC ATTGAACTTT GAACCTTGCC 60
CTTCCCTTCC CTCTGCCCAG CCACTATCAC GCACAAACAA TGCCCTTTCC CCTGGTTGAG 120
TCTGTCTGTC CTCCAGTTCC AGCCTCCAAA AAGCTTTATC ACTTTAGTGC CAAAGCTGCC 180
AACTTCAGTG TATATGAACA AACGTACTTA AAGGACAAAA CAAAACAAAA AGACCTGCCT 240
CTCTATTGCC TTTGAAACCT ACCTTATCTT CTTCACTCCC ACACTTTAGA TAAATGTCCA 300
TTTGCCTGCA ACTGTTTTTA TCACACACCC TCTCATTGGC CAGGGTAGTG TCATGGTCTC 360
TGGAATCCTC CAGACTCTGA TTCCAATCCC GGTGACCCTA GGCAGTGAGT TGATCCCTCA 420
AAGCCTCACT TTTAGTCATC TGTAAAAGAG AGTCAGTAAT AGCCTCCAAA TAGCTCACAC 480
TGATTCATCA CCACTGTTGA TGTCAGGGGA TAACTTATGA AAAGTACCTA ATATCCTTTG 540
CCTGCCAGGC CCTTCCTTCC TCCATCTGGG GAATCCAAGG TCTGGGTTTC AGTCTCCATG 600
AAACCTTTCC CAACCAACCG GCTGGAGCGA GTGATTCCTT CCTGCCTGCC TGCACCTCCC 660
TAGTACTTCG AGCGATTATT TGCTGACTCT CAGCTCCATC CCACCCCACC TCCAAACAGG 720
CTGCCCAATG GTCAGAGTCA TGCTGCATTA GAGCCAGGGG GTTAGGAAGA AAGGTCATGG 780
ACTTGGACTT GGACATCACA CTTCAGTGTG ATCTGCATTG GGACTGTGGC TCTGCACCTC 840
AGCTGCTTGG CCTTAGCAAG TCCCCTAACC TCTTTGAGCT TCCTTTTCCT TATTTATAAA 900
ATTGTGATAA CAGTAGTTAT TTTATACGAA TGCTGTGGAG ATTTAAGTAC ATAATCCATG 960
TCAAGCATTT CACATAATGC CCAGCACTCA GAAAGTGCTT AATAAACGGT CCCTTCCTCT 1020
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