| Tag | Content |
|---|
EnhancerAtlas ID | HS092-37746 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:4855260-4856660 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr9:4856595-4856605 | TTTAATTAGA | - | 6.02 | | 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 | TAGAGCCCCT ACTGCCTAGA ATGGTTCTTC TGAAAAGCTG CTATTTGCGC TGTGTGGGTG 60
GTTACTCATT GAGGGGCAGA GCTGCTCTCG GTGAGCGGTG GGTCTCTTTG CCCTGGGTGT 120
GTGGCTGTGT GGTTGTGTCT AGGAAGTGTG AATCTCCAGT GTAGTGCTGT GGAAGAGAGG 180
GGCAGGGAAA TATGAACTCA AGAGGCGGTG CCTCAGTGCA GCTGCTGCTG TGGAGAGCTG 240
TTGGGCTGTG GAGCAGGACG TGGATCAGCA CTGGACAAGA CTTTGTTCAA GTGCATGTAG 300
ATACAGGACG AGCTTACTCT TCATTTGCTT TTCGTTTTCT TAAGGAGGCT GTTTGCTGGG 360
ATTTAATATT GTCTGTGGTT TTTTTTCAGG TTGTGAGCAT TTTTGCTCTT CAATATCCCA 420
GCTGCCAGAG ACATAGGGAG AATGGGGCTA GAGGTGGGGG AAAGATTCTG AAATGTACCT 480
TAATCTAGTC TCTTACACAG TCTTCCTTGG ACAGGCTGAG GAGTTGGCAG AACATTATGT 540
AAAAAGTGGA ACTAACTTTG CTTTTTCTAA CTGTTCCAAA GGCTACAAAT ACCCCAAACT 600
TGCAAATACA CAGGCCTGCA CACTTGAGCC TGTGTTCCTC CCATCCTTCT CCAAGAGATC 660
AGAAGCAAGC TGAGGGCCCG TAGAAATTCT GCCAGCTGGG GAGGGTGTCT GGTTTTTCAA 720
GCACAGTTGA GTGATTCAGA GTGAAGTAGG CTGGGTGACA TCCTGGGAGC AGAGCATGCC 780
CCAGGCCTGT GTTAGTTTGA GGCAGCAGCA AAGGAGAGAC CAATCTGTTT TCTCCTTCAG 840
ATGCAGAGTG GGTGAGATGG CTGGCTTTTT CCAGGTTGCC GCCAGCTGGA AGCTTTGCCC 900
ACAGATGTGG ACTGTTTATC TGTGGTTTGC TGTGTTTTCT TTTTTCCCTA GGACAGGATG 960
GGGGAGATGG TGGGATGGAT AGAAAGCAAC AACGACAACA GAAATTTAAT TGGTTAGTAA 1020
GACAGGAAAG CCAGCAGGGA AAGCTGACTT CCCTTAATTG CCAAGAATGT TGAAAATTGT 1080
TTCTCAAAAT TACCCCAACT CCTAAATTCT ATCCAGTGCC TCTTTACTGA GAACCTTTAC 1140
AGTGCCTTGT TTGAATAACG GGTTCAGTGA TGGAGAAGAG CCTCTTTACT GAGGCTAAAT 1200
TCTATTCAGT GCCTCTTTAC TGAGAACCTT ATACAGTACC TTGTTTGAAT AACGGGTTCA 1260
GTGTTGGAGA AAAGCATTGC TGTTGAGGTA CTTAAATAAT TTAATGATGG GGAAGGGGAC 1320
AGTGATACAT AAGCATTTAA TTAGACACCA TGAGCAGAGA ATGCTATGGA AACCTGGAGG 1380
GGTGGGAAAG ATCGTTTGGG 1400
|
