| Tag | Content |
|---|
EnhancerAtlas ID | HS002-01054 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr1:206939170-206940400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PBX1 | MA0070.1 | chr1:206939368-206939380 | ACATCAATCAAT | + | 6.44 | | TCF7L2 | MA0523.1 | chr1:206939770-206939784 | TCGCTTTGATGTTT | - | 6.54 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_18640 | chr1:206938558-206940480 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19631 | chr1:206939257-206940450 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_61266 | chr1:206939355-206991151 | HBL1 |
|
| | 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 |
| GH01I206765 | chr1 | 206939241 | 206940345 |
|
Enhancer Sequence | TAAGCCTTCC AGGCCAGGGG ACTTGTGAAC CCTGAAAATT TAAGACAGGT CTCAGTTAAT 60
TTAGAAAGTT TATTTTGCCA AGGTTGAGGA CATGTGCCCG TGACACAGCT TTGTCACACA 120
GCCTCAGGAA GTTCTGATGA CATGTGCCCA AGGTGGTTGG GGCACAGTTT GGTTTTATAC 180
ATTTTAGGGA GACATGAGAC ATCAATCAAT ATATGTAAGA AGTACATTGG TTCCATCCAG 240
AAAGATGGGG ACAACTCAAA GCAGGGAAGG GGCTTCCAGG TCACAGGTAG GTAAGAGACA 300
AATGGTTGCA TTCTTTTGAG TTTCTGATTC TTTTCCAAAG GAGGCTATCA GATATGCATC 360
TATCTCAGTG AACAGAGGGA TGACTTTGAA TAGAATGGGA GGCAGGTTTG CCCTGAGTAG 420
TTCCCAGCTT GACTTTTCCC TTTAGCTTGG TGATTTTGAG GCCCCAAGAT TTTCCTTTCA 480
CAGACTCAGG ATGTCTTCTT CAGTTCAGGA TGGACAGCCT CAGAGTAGAG AGCTTCAGGC 540
CCCCTCTCCT TATCTTCTGC TAACCTCCAT TCTTACTCCT ACCCTTTCAT CTCAGAATTT 600
TCGCTTTGAT GTTTCCCACT TCCTTCCTAT GGTTACTTTA ACCGAAGTGA GTCAGGTCTT 660
ACTGAAAAAC TGACCACAGC CTGTCCGCTC CCAGCCTTCC CCAGACCAGG GCTGCCCAGG 720
CAGAGCGTGA GGGGGACTAG TGTTTACTCA GCTCATTTTT TTCCTCCTCT CTCCTCTAAG 780
TCACGGGGCT TTGAGTAGGG CTTCCCCAGC CACCGTGCCC CTCCCAGCAG ACCGCAGTCA 840
GAAGCCAATC TCACATTTGT CTGGTGGCTC AGAGAGGGGA CAGAAAGAGC AGCAGCTTAT 900
GTCCTTGGCT ATCCTCTCAA GTGGGCTAAT TTGCTTATTT TCAACTCTGT TGGGTCCAGC 960
CCTGTTGCCT CTGATCTCAG CTCAAAGAGG ATTTGGCGGG AGTTTTTGGT TGTGATAACC 1020
AATAACAACC AACTATACGC ACTGCGAACA TCTCCTAGTG CCAGAAGCCC TGTTAGCTCA 1080
TTATCTTAAT CCTCAGGATA ACCCAGGCAA TTTGTATTCA CCCTAAAAAC TTCCCCTGGC 1140
CGGGTGTGGT GGCTCACGCC TGTAATCCCA GCAATTTGGG AGACTGAGGC AGGCGGATCA 1200
CTTGAGGCCA GGAGTTCCTA ACCAGCCTGG 1230
|
