| Tag | Content |
|---|
EnhancerAtlas ID | HS098-43771 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr4:170266220-170267660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr4:170266663-170266674 | CATGAGTCACT | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr4 | 170266400 | 170266800 | | chr4 | 170266800 | 170266979 | | chr4 | 170266348 | 170267006 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I169345 | chr4 | 170266219 | 170267320 |
|
Enhancer Sequence | GGGGTGAGAA CTAGTATTTA TTACCTACAT ATTTATGTAT CTATCAGATA TATTTTTGTT 60
ACATTCTGGA AATCAATAAC ATCAGTGAAA AGGAGAGAGA ATTCTTACCC CCTGTTCCTT 120
TAACCTTTAC CGAAGAAAGG CAATGGGTGG GGCAGCACGT TTTATGGGCA GTTTGTCAGA 180
TCTCCAAGAC TCTAAGGAAT TACAGTGACC CCACACAGCA GGCACAGGGA CTGTCCAGCC 240
ACAGGTGGAT GGCCAGGGAT ATCCGCAGGG GCTGAAAGAG AAGCACTCCC ACCAGCTTCT 300
GGGTTTGGTC AGCAACTGGT GAGAGACTGG ACAGCTGAAG AATGTGCCCC CAGTGGAACA 360
TTTTCAATAA CCATTAGGCT TCCAATAAAA AGAAGTTAGA AGCAACAGTG TGAAAGATGT 420
GACTGTTTCC TCAGAGGTCA AAGCATGAGT CACTGTGAAT TAGGCAGTCA AGGGATGGCC 480
CTTTTTTGTG CACTCACCCC CCTGTCATCA ACCAGAGTCA TTGTTCTTCT GAATAACCCC 540
CCCGTTTCAA TGCCAGGGGG TTCACATCTG GTGGTGACAG GAGAGTTTTG CCAACAGGAT 600
TCCAAATGTC AGCAGGCTGA CTGGTCAATG CTTACTCAGG CAAGCCTTCC CAGTGAAGCC 660
ATAATTACCT CCCGCTCTCA GAATAGGATT AACAAATGCA GTTATTTGTG TATGATCCTT 720
TTACATACAA CCTCATGCAT TTTACTCATG CCAGTTAATA TTTCCCATTA GAAAAATCCT 780
CTTATATGAA TGCCATGATA AATAAATTAT TGGCATTTTA AAAAAACCTT GTTAACCAGA 840
AATGGCCGCA AGGGTGAAAG TGTTTATACC TTCATACAAT AATGCATTTC TCTTTTTATT 900
TTAAGACTGT TTCCTTTCAT TCAGTTTATG AGTAAGGCTG GGAATCAATT AAGTTTTAAG 960
TGCAAAGACA AGGGATATGA TTCCTAAAAA TAAAAGAAGA TAATTTAGGT GTACTTTAGA 1020
GGTAATTATA GCAGGATTTT GTTCAAAAGT TTCCCAATAT AACTATGTGA CTTGTGAAAA 1080
CCTATCTCAA CACTAGTTTC ATCACCTATA AACTGGAGGT AATTCACGCC AACCTCACAG 1140
AGATGTTTTG ATTCAGTAAT GAGTCTTGTC TTTTGTGGCA GTTCTAGAAG CTCCAAGGAC 1200
AGGTGCTGCC AACTGTCCCA ATTTAGCCTG TGGCAGTCCT GCAAGTGAAA ATCTCAAGTT 1260
CACCCACTGG TCCTGGTCCT TATCAGGAAA AGGGGGCTAA ACTGATGTTT CAAACTAAAT 1320
ATGATTAACC AGCTGGCGAT TATGAGCAAG GCAAACACTC TCCAAGCCTC CCTTAATCTA 1380
TAAAATGAAT GTGGAGAGGG AAGTAGTAGC TAGATGATAT CAGAGACACC TGACAGCATA 1440
|
