| Tag | Content |
|---|
EnhancerAtlas ID | HS037-13544 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr15:99663550-99664700 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr15:99664038-99664053 | TGCTGAGTCACGGCG | - | 7.1 | | Zfx | MA0146.2 | chr15:99663928-99663942 | CAGGCCCCGGCCCC | - | 7.1 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_01751 | chr15:99662632-99667579 | Aorta | | SE_26071 | chr15:99661754-99671456 | Duodenum_Smooth_Muscle | | SE_26894 | chr15:99662771-99666936 | Esophagus | | SE_41005 | chr15:99662692-99667652 | Left_Ventricle | | SE_48129 | chr15:99662590-99667752 | Psoas_Muscle | | SE_49228 | chr15:99663000-99666997 | Right_Atrium | | SE_51485 | chr15:99658952-99667594 | Skeletal_Muscle | | SE_54502 | chr15:99644762-99680377 | Stomach_Smooth_Muscle |
|
| | 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 |
| GH15I099122 | chr15 | 99662701 | 99666855 |
|
Enhancer Sequence | CTGGGATGTG GTTGAATACT GACCCCAGAA GCGATGCCCG GAAATGGCCC AGCACTGCCA 60
CGTTACCTCC TGTTATCCTT CCTGTGAAGC CGGTGGTCTC ACCTTTCCCG TTCAGGTGGC 120
GTTGCTGGTC ATGGGAATGG AACTCCCCTC TGCCCCCTCC CTTCTGTTCC CTGGTCTTCC 180
CGGTGACTGA CCAGCCACGG GCCCGCATCT GGGGTGACCC AGGCAGTGCG TCCACTCTGT 240
GTGGAGCTTG GCTTCCTCTG TCGCAGTGAG GAGTCGAGGG AGGCGGCTCT GCGGCTCCTT 300
CTCCAGCTCC GGAGCCTCCC TTTCTTCTCT GCACTTCTCC ACCTGCTGTT TGCTAGGAAG 360
CACCCCGTGA ATCACCCACA GGCCCCGGCC CCGGCCCCAG CAGGCTCCCG CACAGACACG 420
GCTTCTGGGA ACATCCTGAC AGTGCCTCAT TTATGGGGCT GCACAGAGCA GTGGCCTTGT 480
GCCCACGGTG CTGAGTCACG GCGGATTGTT CAGCAATTCC ATTAGGATAA TCTATCCCAG 540
ACAGAGAGCC TTGCCTTGGA GCCTGCTCAG GACGCCGGGT GGCCCATTAG GGCCTGGCGC 600
CTGGCCAGAG GCCACATGAC AGCCGGCTTC TGCACTGTGG GTTTGTCCTG GGCTCCTTAA 660
TGAGGCCAGG GACTTGAGTT TTCTTGCACT TTTGCTTATT TTCCTGCATA AGGGGCCACC 720
AACCTGTGGA GCTGTGTGAA ATGCCCACAA TAGCCCATGA CTCAGGGGAT TGGCATTTCT 780
CACAGTCCCC GAGGCTTGGG GGCAGATTTC CTCCACCGCT CTCAAAATAA CCAGGTTTGA 840
TTGCAGCCTC AGAGAACATG CTACCCATTT CTTAAAGTGG TACGAACCTA TTCCTTAAAA 900
ATGTCCCTTG CAGAGCTTTA GAGGAAGTCG TGGTTTCTGG CTTCTCCTCA GAGTCTTGTT 960
GATGCTTTCG CCGTGTAGTC CTGGGGCTGT GCGGAAGGAG GGTGGCTGCC ATTGGGCTGG 1020
ATGTGCTACC CAAAGCATGA ACTCAATGGC CAGTGCCCAG CCGGGTGCTC ACAGATAGTA 1080
AAGGTGACAT GTGTCGCTGC CTGCTAGGAT CCGGCCATTG AGAAGGGACA CAGATGAGGG 1140
ATAGCTCCTT 1150
|
