| Tag | Content |
|---|
EnhancerAtlas ID | HS138-19321 | Organism | Homo sapiens | Tissue/cell | MSC_BM | Coordinate | chr2:10798090-10799290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr2:10798148-10798159 | TGCTGAGATTT | - | 6.32 |
| | | 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 |
| GH02I010658 | chr2 | 10798417 | 10799520 |
| Enhancer Sequence | ATGGCAGCCA TTTGCTTCAT CGCTTTGTTA TGAACACAAT GAACACCCTT ACTCAAGGTG 60
CTGAGATTTG AGATTCTTTC CAGAAAGATC TCTTAAATAA TCCTTAGAGT ATACATTTTA 120
TGAATTCAAC CCCAAGATTA ATTTGTAAGA GCTACTGAAC ATACTAAGAA AGAACAAAAA 180
ATGAAAGCCC ATAAGAATTT AATTTGTTCA ACAAATATAT ACTGAGGGCC TATGTACCAG 240
GCAGTGTCAT AGCAACAGAT ATAAACAAAA ATGAAAGACA TAATCAGGAA CAGTCCTAGT 300
AGATCAAGAC AGATGGTGGT GGCAAGGCTA TGACTTCTTG GGAGAAGGGA GAATCTCTTC 360
GGACCCGTCA CTAGAGGCAA GGAAGCCTGG GAAAGCTCCC CTAGGATTAA GTCCCAGGTG 420
ACAGATGCCC TCTAGCCCAT GATGACAAAG AAAGTAAATC CTCCAAGGCA GGGTTTCAGA 480
CCTCTTGTAG GAGGCAAGTG TACAGGCTCT GCCTTGAAGG AAAGAAAGAA GTACTCCTCA 540
GACTAGCACT GCTAATGCAT GTTCTGCTGA CCACTCATGG CATGTGCTAT AGTTAATGAT 600
GCTATATTAA AAAAAAAAAA GTTCCTTGAA CACACAAATT TTGGAAATAT TTATTAAACA 660
TATTTCTTGT CTGCAAGAAT TCCTGAGAGC CTTCATTAAA ACAGTATTGA AACCCACTGT 720
CAATCTTCAA GAGTAAAAGT CTGGCAGACT CCCAAGACTG TCTGACCACA GAATTCTGTT 780
GCATAGACTC TGAAAAATGC TGTTCCAAAC CACTAACAAG AGAATACCTA TGGCCAAGCC 840
CGGTGGCTCA CGCCTGTAAT CCCCACACTT TGTGAGGCCA AGGGTGGGGG GATCGCCTGA 900
GCCCAGGAGT TCAAGACCAG CTTGGGCAAC ACAGTGAGAC CCTGTCTCTA CAAAAAGTCA 960
AAAAATTAGC CAGGTGTGGT GGTGCAGGCC TATCCCACTG CAGCTCTAAG TCCACAGCAC 1020
TGCAGACTGA CCAAGGCAAG AGTCAAGATT TCTCAAGGTG TGGAAGAATC CAGCATTCTG 1080
GAATACCCTC TGGTCTGGCT AAAATAGTAT GATCTCATTT TCTGTTCCTG CAGTGTATTT 1140
CTCATGACAC ATACACACAC CACTGAAATA CCAACTTACA TGTGGTTTCC AAATTAAACA 1200
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