| Tag | Content |
|---|
EnhancerAtlas ID | HS098-56659 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr9:4855170-4856560 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr9:4855630-4855641 | GTCTGTGGTTT | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_02232 | chr9:4855153-4857192 | Aorta | | SE_12818 | chr9:4855765-4856084 | CD34_fetal |
|
| | 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 |
| GH09I004854 | chr9 | 4854434 | 4856991 |
|
Enhancer Sequence | AAAATCATTT TGTCCCGGGG AAAAAAAAAG CCTCACTGCA GATAATCATT CTCTATGTTA 60
GGTGTTAAAA TCCTTTACAC AGGAGTTGCA TAGAGCCCCT ACTGCCTAGA ATGGTTCTTC 120
TGAAAAGCTG CTATTTGCGC TGTGTGGGTG GTTACTCATT GAGGGGCAGA GCTGCTCTCG 180
GTGAGCGGTG GGTCTCTTTG CCCTGGGTGT GTGGCTGTGT GGTTGTGTCT AGGAAGTGTG 240
AATCTCCAGT GTAGTGCTGT GGAAGAGAGG GGCAGGGAAA TATGAACTCA AGAGGCGGTG 300
CCTCAGTGCA GCTGCTGCTG TGGAGAGCTG TTGGGCTGTG GAGCAGGACG TGGATCAGCA 360
CTGGACAAGA CTTTGTTCAA GTGCATGTAG ATACAGGACG AGCTTACTCT TCATTTGCTT 420
TTCGTTTTCT TAAGGAGGCT GTTTGCTGGG ATTTAATATT GTCTGTGGTT TTTTTTCAGG 480
TTGTGAGCAT TTTTGCTCTT CAATATCCCA GCTGCCAGAG ACATAGGGAG AATGGGGCTA 540
GAGGTGGGGG AAAGATTCTG AAATGTACCT TAATCTAGTC TCTTACACAG TCTTCCTTGG 600
ACAGGCTGAG GAGTTGGCAG AACATTATGT AAAAAGTGGA ACTAACTTTG CTTTTTCTAA 660
CTGTTCCAAA GGCTACAAAT ACCCCAAACT TGCAAATACA CAGGCCTGCA CACTTGAGCC 720
TGTGTTCCTC CCATCCTTCT CCAAGAGATC AGAAGCAAGC TGAGGGCCCG TAGAAATTCT 780
GCCAGCTGGG GAGGGTGTCT GGTTTTTCAA GCACAGTTGA GTGATTCAGA GTGAAGTAGG 840
CTGGGTGACA TCCTGGGAGC AGAGCATGCC CCAGGCCTGT GTTAGTTTGA GGCAGCAGCA 900
AAGGAGAGAC CAATCTGTTT TCTCCTTCAG ATGCAGAGTG GGTGAGATGG CTGGCTTTTT 960
CCAGGTTGCC GCCAGCTGGA AGCTTTGCCC ACAGATGTGG ACTGTTTATC TGTGGTTTGC 1020
TGTGTTTTCT TTTTTCCCTA GGACAGGATG GGGGAGATGG TGGGATGGAT AGAAAGCAAC 1080
AACGACAACA GAAATTTAAT TGGTTAGTAA GACAGGAAAG CCAGCAGGGA AAGCTGACTT 1140
CCCTTAATTG CCAAGAATGT TGAAAATTGT TTCTCAAAAT TACCCCAACT CCTAAATTCT 1200
ATCCAGTGCC TCTTTACTGA GAACCTTTAC AGTGCCTTGT TTGAATAACG GGTTCAGTGA 1260
TGGAGAAGAG CCTCTTTACT GAGGCTAAAT TCTATTCAGT GCCTCTTTAC TGAGAACCTT 1320
ATACAGTACC TTGTTTGAAT AACGGGTTCA GTGTTGGAGA AAAGCATTGC TGTTGAGGTA 1380
CTTAAATAAT 1390
|
