| Tag | Content |
|---|
EnhancerAtlas ID | HS113-37219 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr9:4855240-4856570 |
Target genes | |
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 | TCCTTTACAC AGGAGTTGCA TAGAGCCCCT ACTGCCTAGA ATGGTTCTTC TGAAAAGCTG 60
CTATTTGCGC TGTGTGGGTG GTTACTCATT GAGGGGCAGA GCTGCTCTCG GTGAGCGGTG 120
GGTCTCTTTG CCCTGGGTGT GTGGCTGTGT GGTTGTGTCT AGGAAGTGTG AATCTCCAGT 180
GTAGTGCTGT GGAAGAGAGG GGCAGGGAAA TATGAACTCA AGAGGCGGTG CCTCAGTGCA 240
GCTGCTGCTG TGGAGAGCTG TTGGGCTGTG GAGCAGGACG TGGATCAGCA CTGGACAAGA 300
CTTTGTTCAA GTGCATGTAG ATACAGGACG AGCTTACTCT TCATTTGCTT TTCGTTTTCT 360
TAAGGAGGCT GTTTGCTGGG ATTTAATATT GTCTGTGGTT TTTTTTCAGG TTGTGAGCAT 420
TTTTGCTCTT CAATATCCCA GCTGCCAGAG ACATAGGGAG AATGGGGCTA GAGGTGGGGG 480
AAAGATTCTG AAATGTACCT TAATCTAGTC TCTTACACAG TCTTCCTTGG ACAGGCTGAG 540
GAGTTGGCAG AACATTATGT AAAAAGTGGA ACTAACTTTG CTTTTTCTAA CTGTTCCAAA 600
GGCTACAAAT ACCCCAAACT TGCAAATACA CAGGCCTGCA CACTTGAGCC TGTGTTCCTC 660
CCATCCTTCT CCAAGAGATC AGAAGCAAGC TGAGGGCCCG TAGAAATTCT GCCAGCTGGG 720
GAGGGTGTCT GGTTTTTCAA GCACAGTTGA GTGATTCAGA GTGAAGTAGG CTGGGTGACA 780
TCCTGGGAGC AGAGCATGCC CCAGGCCTGT GTTAGTTTGA GGCAGCAGCA AAGGAGAGAC 840
CAATCTGTTT TCTCCTTCAG ATGCAGAGTG GGTGAGATGG CTGGCTTTTT CCAGGTTGCC 900
GCCAGCTGGA AGCTTTGCCC ACAGATGTGG ACTGTTTATC TGTGGTTTGC TGTGTTTTCT 960
TTTTTCCCTA GGACAGGATG GGGGAGATGG TGGGATGGAT AGAAAGCAAC AACGACAACA 1020
GAAATTTAAT TGGTTAGTAA GACAGGAAAG CCAGCAGGGA AAGCTGACTT CCCTTAATTG 1080
CCAAGAATGT TGAAAATTGT TTCTCAAAAT TACCCCAACT CCTAAATTCT ATCCAGTGCC 1140
TCTTTACTGA GAACCTTTAC AGTGCCTTGT TTGAATAACG GGTTCAGTGA TGGAGAAGAG 1200
CCTCTTTACT GAGGCTAAAT TCTATTCAGT GCCTCTTTAC TGAGAACCTT ATACAGTACC 1260
TTGTTTGAAT AACGGGTTCA GTGTTGGAGA AAAGCATTGC TGTTGAGGTA CTTAAATAAT 1320
TTAATGATGG 1330
|
