| Tag | Content |
|---|
EnhancerAtlas ID | HS138-44107 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr9:127104000-127106190 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr9:127105672-127105682 | GGGGATTAGC | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 127104003 | 127104697 | | chr9 | 127104720 | 127106158 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH09I124340 | chr9 | 127103109 | 127107948 |
| Enhancer Sequence | TGAGCAGGGT GTGTGGGTGG GCTCGGGGGA GGGCAGTGGA TGTAGGAGAG AATTTGGAGG 60
GAAGTCAGTG TCTTTAGCCA TAGGAGACAA GACATGTTAA GTCCAAACTC TTCTGAGACA 120
GGAGGAAACC TGCTGGTGTA GGGCCCTGTG TGCCTGCACA TTCCGAACAG CCCCGGGGAG 180
GGTGCGTGCC TGTTATTTTG CGGAGAAGAC GTTAAATCCA GGTGGGGAAA GCCCCGGGTG 240
TGGAGAGTTG TTGAGTGGCG CAGAGCCACT GTGCTGCTGG TGTGTGTCCC CCAGGAGGAG 300
TCGTGAGTTC CAGTCTCTCC AGGACTCCTC TAAATCCAGG CAGGTGGCCA CTCTGGCCAC 360
CAAGGTCGCT GAGGCTAGCA GTAGAGTCAC GCCCATGTCA CCTGCTAACC CGGCTGTCCC 420
TGGGCTCAGG GCTCCAGCGT CACCGCCCTG CCCCCACTTG CCCTAAGGTC TGAGGAGGGG 480
ATGCAAACCC ACCTGTAAGT GGGCATCGTT CACCCGGTGT CAGATCCTGA GGGGAAGAGA 540
CAGGCGTTCT AGGTCTCCCA AGGCCCAGGC TAATGCCCGC AGCATAGTGG ATGGTCGGGG 600
AGCACAATTT TGAATTAGAG CACGTGTCTG TGTGTAGGCA GCTCACTTAC CAACTCACTT 660
TCATCCAAAT CCCAGCTCCA GGGCCCACCC ACGGAAGGAT CCAGGCAAGT CAGCCCCTCC 720
CGGGTGGGCC TCAGGTGTCC CATATGTAGA ATGAGTGGCC AGCCCACCTT GTCATAGTGA 780
GGAAGGAATG AGGCCCTAGG GGTGAGGTGC CCGAGTCAGA GAAGGCCCTC GGGCCTGTCC 840
ACCAGCTGCA GGCCAAGCAC GGGCACTTCT GCCCGCCTCC GGCACGAGGC TCCTGCAGCT 900
TGCCACATTT CCCTTTTTGC TTTGGCCAGC GGGAAGCCAA AGTGCAGCCC AGCCTCAGTC 960
TCCGAGGAGG CTCCACTTTG TCCTCCTTTC CTCATGTGTC TTGTCCCTGG GTCAGATGGC 1020
TTTTCGTTTC TTTTTCCATT CTGCTTTGTG TTTTTGTAAG CTGCTTCCTG TCTCCCATGA 1080
ACCATGGGCT CTCCACACAT AAACACACAC ACAGCATATG AACACACACA CAGGCTGGCC 1140
AGGCTGACAG AGCTGTGCCC ACTTCCCTGG GGCTGGGGCC GGGAGGCCAG CAGCTGGCTC 1200
CCTCTGCCTG TGCCAGGCCC TCCACTTGAG AACCGGCCCT GTGGTTCCCA GCCCCGTTCC 1260
CTGCCTCAGT CTTTGTCTCG GCTCTGCAGA GGCAGGCACA GCCCATCCTG TGCCAGGCCT 1320
CACTGAATTC TGGCTCGGGC AGTCCTCCTC CGAGTCCTCA TTTGTGGGCA CCTAAATGTG 1380
CATCTCACAA GGCAGTCCCG CCTTCGTGAC TCCCTGGCAT TGAGGCTCGG GTTACGCCGA 1440
GCTGACTCAT TTGTTGGAGT GAGTGGGGCT GTGCGGCTCG CAGCTGGGGG GGCTGGACCA 1500
CAGCCGGGGG GCGGTGAGGG GACGGATCGC AGCCGGGGGG TGGTACGGGG GATGGATCGC 1560
AGCTGGGGAG GTACCGATCG CAGCGAGGGG TGGTGTGGGG GGACAGATCA CAGCCAGGGG 1620
TGGATACCAG TCAGCAGTAG GAAGTGAATG AAACACAGCA GTCAAGCCCT GAGGGGATTA 1680
GCGTCCTCAG GGACATCAGG CGCTGACCTA ACCCTAGCAG CCCCGGCCTC ACACAGCAGC 1740
AGGCTGCTGT GGCCACCCAT AGCCGGCCCA TCCAAGGGTA ACGGGGCAGG GGCTCTGTGC 1800
CAAGTGACCC CCTCCCCACT CCTGCAGTCC CTAAAGGGGA AGGTGAAGCA GGCGTTTCCC 1860
CAGCAGACAG GGAGGAGAGC CACATCTGAG CCCACGGCCA TGTAATTGGA AAGAGGCCTC 1920
CCGCAGTCAC GCCCGGAGCC TCCCGCCCCA CAGCCTGTGG TGTCTTCCAG GGGCACCAGC 1980
CTGAAGAGCT GTGACAAAGC CCCCTGCCCT CTCTGGACAA CAGCTGAGGA TCCTGCACAG 2040
GGCACATACC CAGGTCACCT GGGCCCTGGT GACAGACACA GCCGGAGAAA ACCTGCCCTT 2100
CCCCAAGCCC CAGCACAGCC CGGAAGGCTC AAAAGCCCCT GTGCTCATCC CTGTGGCTGC 2160
AGTGACAGAT GCCACCACGC CGATGGCTTC 2190
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