Tag | Content |
---|
EnhancerAtlas ID | HS098-28780 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:9330920-9332230 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr2:9331153-9331168 | ATTGCTGTGTCATAT | - | 6.22 | Spz1 | MA0111.1 | chr2:9331067-9331078 | AGGGTATCAGC | + | 6.32 | ZNF410 | MA0752.1 | chr2:9331162-9331179 | TCATATTATGGAATGGG | - | 6.11 |
|
| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_02003 | chr2:9328555-9332273 | Aorta | SE_31918 | chr2:9330820-9332212 | Gastric | SE_45636 | chr2:9329406-9334678 | Osteoblasts | SE_55827 | chr2:9329113-9333467 | u87 | SE_67923 | chr2:9329113-9333467 | u87 |
|
| 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 |
GH02I009189 | chr2 | 9330018 | 9334042 |
|
Enhancer Sequence | TTTTGAGCAA AGAAGCTGGA GTATCTGTGG GGTCTTGTGC CCTGCTGAGG GAGTCTTAGA 60 CTTGGGAAGT ATAGAACCCC TGGTAGTCCA GCTTGCGAGT CAAGTGGGCT GAGATCCACT 120 CAGCCAAGGG CCCAATCCCA CCCTATTAGG GTATCAGCAG CTTTCTATCT GATGCACAGT 180 GGTGGGGATG CATGTGGAAG GCATGCTCTT TGCTTCTGCC AGCCCCAGGC TGGATTGCTG 240 TGTCATATTA TGGAATGGGG CACAAAGGGG GCATTGATTT GCTGGCAATC CTGCCATGGA 300 ATCCCTTGGT CACGGCTTTT CCATGCCCTG TCTCCAGCAT ACTCAGACTG ATCCAGTGTG 360 CCCAACCAGC CGTTTCCACA GGTCTGGCCC GGCCAGGGAC CTTCTTGCCA CATTCTGGGC 420 TCTGCCCACT GGAGAGTTCA GGACAGGACC CGGGTGCAGA CCGGAGGCCC AGGCGCAGAG 480 TTGTTATGCT CAGGGCCATA TGGAAAATGT GAACAGGGCC TGAACAAACT GCACAGCTCA 540 CTTCTTGGCA TTTGCAAGTG GGACTCACCA AGATGCAATG CAGAGGCGGC CAGTGAGGTC 600 AACTTTGGCT GAGAACCCCG AACAGACTGG GAGAGTCCAG GAGAGAAAGG AAGGGACACT 660 GGAGCAAACA TAACGGGGTG TAGCCCTGTT TTAAAAACAC CAACAGAGAA AGCAACCTTT 720 GGAGGAAAAG TGCATGGCTC CAAATCCCAG GGGGGCCCAC TCTTGTCGGG GGTCTGATAT 780 CTGACCCCTG GGCTGCCCAG AAGCATTCAC TAAATGCTGC TCTCCAACCA AGTTAAAAGA 840 AAACAACTCC CAAACTCTTT GCAAAGAGAG TCACACACAT GGCCTTGCAG ACTTTGGGAA 900 TTCCGCAGAA CTGAGAAAAT GAAGTCTCTG TTTCGAGCCA TGACTAGGTC TCTTATATGA 960 CTAAGGGTTA TTACTTCTGC TTAGAGGCAG GAAACATCCA CAGCTCCAAA TCCTACAGGC 1020 CAACCAACCA CTCTCTGTGT GGCGGTTAGG CAAGCACTTT CAGAGTGAAT GTTGGGCACT 1080 TACAGATCCC TTGGGAACTT TTTGCTCTCT GATCACAACT CTGCAAGTGG TTCCCCAGAG 1140 ATGTGAAAGA GCAAGTGCTC TAAGAAGGCG CCTGCTCACT TACAAACCCA CTCACCTCTA 1200 AGATTCGCCC CACACATTCA CAGACCTGGA AAGAAATTCA AAGTCCTTTT TTTTTTTTTT 1260 TTTTTTGAGA CAGAGTCTTG CTCTGTCGCC CAGGCTGGAG TGCAGTGGCG 1310
|