| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08028 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:125110450-125111560 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr12:125111271-125111291 | GGTAGGGGGTTGGGTGGGAG | - | 6 | | ZNF263 | MA0528.1 | chr12:125110724-125110745 | TGCCCTCCACACTCCTCCTCC | - | 6.01 | | ZNF263 | MA0528.1 | chr12:125110727-125110748 | CCTCCACACTCCTCCTCCTCT | - | 6.13 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_09620 | chr12:125108910-125112362 | CD14 | | SE_23633 | chr12:125110096-125111555 | Colon_Crypt_1 | | SE_29720 | chr12:125110106-125112177 | Fetal_Muscle | | SE_34780 | chr12:125108082-125112444 | HeLa | | SE_57235 | chr12:125109943-125112300 | VACO_400 | | SE_57418 | chr12:125110264-125111017 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 125110562 | 125110683 | | chr12 | 125110878 | 125111184 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I124625 | chr12 | 125109896 | 125112430 |
|
Enhancer Sequence | AGTGTGGCAG CCTCTAGAAG TTGCAAGAGG AAAGGAATGA AGCCTCCTCT GGACCCTCCA 60
GAAGGAACCA GCCCTGCCAG TGCCCTGACC TCATCTCCAT AAGCTCCACT GGGACCTTCT 120
GCCCTCCAGA ACGGGGAGAT AACAATATTG TGTTGCTTTA AGCCTCTATG TTTGTGGTGA 180
TTTGTTCAGC AGCAATAGGA AATCCACACG TCATCCAAAT GCCCTCCTTT ACAGAAAGCT 240
TCTGAACCCG CTCTTGCCTC GGTTGGCAAA CTTCTGCCCT CCACACTCCT CCTCCTCTGG 300
GATGGGTGGG GACAAGTCCT TCACTGGGGT CAGGTTGCCC CAAAGCCTGT CTCCTGGACT 360
TGGAGGCTGC TCCCTCCGAC CTCGGCACCC CCCAAGGGCC AGAGGCCACC ACCTCGAGCA 420
GCCAGCGGGT AAGAGCCAGC CTGCAGGGTG GATACTAAAT ACAATAGGTC TGTGACCACA 480
CACGGCCCCA CCCCCAGGGG CCCAGGCCCC GCTGACCTTC CCACCCCGGG GCACACCCAG 540
CTGCTTCCTC AAAGCCACAG CCCTTTCCTC CAGCCCAGCC TTTGCCCTGG CCCTTTCCTC 600
TTCTGCTCCT GACGTGCCTG ACTCATCCAG CAAGTTCCAG CTCAGAAATC TCTGGGGGAG 660
CCTGGTCCAG CCCCGTTCCA TCCACCCCGC CCTGCTGGCT TCATTTCATT TCATGCACTC 720
AGTAGATGGG CACACAGCTC TCCTCTGTTC TCCTCTGGAA GGCACAGGCA GAGCCCTCAC 780
CTCAGGACCT CCAGAAGCTG ACAATTGGTC GGCGGGAGCA GGGTAGGGGG TTGGGTGGGA 840
GCCTGTGACA TGTTTTAATG AAGTGTAGAC ATTTTAAATA TACAATTCAA AGACTTTTTT 900
AAAAATCTTA AGTACATATG TTTTTAGAGA CAGGGTCTCA CGCTGTGGCC CAGGCTGGAG 960
TACAGTGACA CCATCATAAC TCACTGCAGC CTCGAACGCC TCAGCTAAAG CAATCCTCCC 1020
GCCTCAGCCT CCCAGCCTCC CAAGCAGCTG GCAGTGCAGA TGTGCACCAC CATACTCAGC 1080
TAATTTAAAT TTTTTTTTTT TTTAGAGATG 1110
|
