| Tag | Content |
|---|
EnhancerAtlas ID | HS176-27011 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr3:111641960-111643130 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr3:111642451-111642466 | TGAACTCTTGATCTT | - | 6.07 | | REST | MA0138.2 | chr3:111642133-111642154 | TTCAGTACAGGGGACAGCTCT | + | 6.54 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_00093 | chr3:111641548-111644049 | Adipose_Nuclei | | SE_34247 | chr3:111620068-111657645 | HCT-116 | | SE_36420 | chr3:111641018-111644000 | HMEC | | SE_38241 | chr3:111641509-111644273 | HUVEC | | SE_41017 | chr3:111641695-111644040 | Left_Ventricle | | SE_57425 | chr3:111641957-111642234 | VACO_503 | | SE_57425 | chr3:111642976-111643614 | VACO_503 | | SE_64408 | chr3:111640954-111643763 | NHEK |
|
| | 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 |
| GH03I111922 | chr3 | 111641042 | 111646194 |
|
Enhancer Sequence | GTATACTGTG TCTCCTTTTC TTCATTTTCC AATTAAACAT TCTTCCCACT CCAGTTGGCT 60
TAGACCTCTA CTCCTCCATC AGATTCTCTC CTGTTAAGAC TACTAAAGAC CTCAGTGGTG 120
CCCAGCCTGC TGGGTGCTTT TCAGTCCCCT CATGATCAGA CTCCCGAGCA GCATTCAGTA 180
CAGGGGACAG CTCTTTTCTT GGTGCTTCTT CACTGTCTCC CTTTTGTTTG CCTCTGTGTA 240
CCACAATCTT CTGGTTTTCC ATCTATTTCT CTTACCTCTT TCTCACTCTT TATCTCTCAT 300
CTGAACTCAG TTCTCTTGTA CCCTCATGTC CTTCTATAGC TATGGCTTCA AATAACTTGT 360
ATATGCTGGT GACTATCATA GGGATTTCTC TAGTTCATAA CCCTTTTTGG AATTCTGACT 420
CATATCCTGT GCCTACCTGA CATCCCCACT TGGATATTTC ATGGGTATTT CCAATTGAAC 480
ACACCCATAA CTGAACTCTT GATCTTATCT TTTCCCTTGC CTTCCACCCT CCACCCTCCA 540
TCCTCTAGTT TTTCCAACCA GGAGATTGCA TCTCTATTCA CCTATATGTT CAACAGAAAC 600
CTGGAAATTG ATCTTGACAC GTCTTTCCTT ATCATCCCTA CATTCAGTTG ATTACCAGCT 660
TGTTTCTTGA TTGCTTCAAC ATCTCTGCAT CTCCACTAAC AGCATTCTCT TCTCTATTAT 720
GAAAATCTCT TATTTAGTCT ACTTCCACTT GCTTTCCTTC AATCCATTCT CTTCACAGCA 780
GCCAATGTGA TTAAAAAGAA GAAATTAGAC CATATTACTG TGGTTTGCAT CACACTGTAC 840
TTGACTATGC ATCCAAATTC CGTAGTGTGA TCTGTCACCA GCCTTTCTGT CACCACCCTC 900
CCATTCTTCA CAGCACTCTC AGAGTCACCT TCCTTTCTAT CTTTCTGTTT GTTAAAAGAT 960
TCATCCTCCC CCAACCCCAG TCCTTTGCAG ATACTGTTTT CCCCTACCTG GAATTCCCTT 1020
CCTCATATTC CATGCCTCAT TGGTTCTGTC TTTCAGGGCT CAAGATCAGT GTTAGTTTTT 1080
CAGAAAAGCC CTCCTAGACC TTTCCAGTTC GGGTTAGATT TTCCCTGTTG TTCTTTTTAC 1140
AGATAAACAT TTTATAATTT ATGTTTGTTT 1170
|
