| Tag | Content |
|---|
EnhancerAtlas ID | HS138-29618 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr4:26289610-26290990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:26290611-26290629 | TATTCCTTACTTCCTACC | - | 6.02 | | NKX2-3 | MA0672.1 | chr4:26290930-26290940 | ACCACTTGAA | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr4:26290802-26290817 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09973 | chr4:26287910-26292066 | CD14 | | SE_59358 | chr4:26286647-26326108 | Ly3 |
|
| | 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 |
| GH04I026287 | chr4 | 26288824 | 26291821 |
|
Enhancer Sequence | CTCAATGATC CTAAGATATT TGAGTACTTG AATATCCTTC AATGATAACA TCTGGGAAGA 60
GTATAAAGTC TGATATTAGT CCTCAGTAGT GCTCTCCAAA AGGATGGGTA GATAACTACA 120
GACATTTTTA ATTACATATC ACTGAGTAAC AAATTACCTC CAAATTTAGG AGCTTAAGGC 180
AAGAATAAAC ATTTATTCTC TCACAGAGTT TCTCAGGGTC AGGAATCCAG GAGTGGCTTA 240
GCTGGGAGGT TCTAGCTTGG GATCTATAAA GGGATTGTAG TCAAGAAGTT GGCTGGACAT 300
ACAGTCTTCT GAAAATTTGA CTAAGGCTGA AGAATCTGTT TCCAAGGTGG CGCTCTCATG 360
GCCGATGGCA GAGTCTTCAG TTGCTTATCA CAGGGACTTC CTTGCAGAGC TGTTTGAGTG 420
CCCCTCTGGC ATGGCAGTTG GCTTCTTCTG CAATGAGTGA TCTAAGAGCA AGAGCAAGGA 480
GGAAGCCACA ATGCATGTAA TGACTTATTC TCACGGGTTG CACATTGTCA CTGCTGCCAC 540
ATTGAATTCG CTAAAACTCA GTTACTGACT ACAGACCACA CCCTAGGAGA GAAGAATTAG 600
GCTCCACTTC TTGAAAGGAG TATCAAAGAA CTTGCAAATT TATTTGTGAG TTTATTTTAA 660
AAGCCCTCAC AAACACGTAT TCTTTAAACT AGAGTGGCTC AGCCCTGCAA GACAGGGAAG 720
TTATAACAAC CAACATTTCT AGAGTGACTC ACTGTTTAGA AAGTATTTCC CCATGTTTTC 780
TCATTGGGTT GTCACAACCC CCCAGTGGAA CAACAGCATT AATATCCCCA CTTAAAAATG 840
AGGAAATGGA AGCGAGGTCA CTTTTGTACA GTTATTTAAC AAGTAAGTTG TATAGCTGGG 900
GATTAAGCCC AGCACAAAGC ATAAGGCCTT TTCACCATCC TTCAAATGAG AAACTTGGCA 960
TGAAGGCCTT TGCACAGAAA AGTTTCATTA GGAAGATTGA CTATTCCTTA CTTCCTACCA 1020
ATTGTTTTTA CCTATTTTAT TAAATTTTTT TATGTTTAAC TTACATACTT CCAAAATTAC 1080
TTGAAGCAGT TTACAAATAA AATGTTTAAG AAAGAAAGAG GAGTAGGGCT GGGCCTGGTG 1140
GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGTG GACAGATCAC TAGAGGTCAG 1200
GAGTTCAAGA CCAGCCTGGC CAACATAGTG AAACCCCATC TCTACTAAAA ATACAAAAAT 1260
TAGCTGGGCA CAGTGGCAGG TGCCTGTGAT CCCAGCTACT TGGGAGGCTG AGGTGGGAGA 1320
ACCACTTGAA CCTGAGAGTG GTATGCAGGT CAAACCACTG CACTCCAGCC TCAGCGACAG 1380
|
