| Tag | Content |
|---|
EnhancerAtlas ID | HS055-00699 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr1:206939340-206940750 |
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 | GGTTTTATAC ATTTTAGGGA GACATGAGAC ATCAATCAAT ATATGTAAGA AGTACATTGG 60
TTCCATCCAG AAAGATGGGG ACAACTCAAA GCAGGGAAGG GGCTTCCAGG TCACAGGTAG 120
GTAAGAGACA AATGGTTGCA TTCTTTTGAG TTTCTGATTC TTTTCCAAAG GAGGCTATCA 180
GATATGCATC TATCTCAGTG AACAGAGGGA TGACTTTGAA TAGAATGGGA GGCAGGTTTG 240
CCCTGAGTAG TTCCCAGCTT GACTTTTCCC TTTAGCTTGG TGATTTTGAG GCCCCAAGAT 300
TTTCCTTTCA CAGACTCAGG ATGTCTTCTT CAGTTCAGGA TGGACAGCCT CAGAGTAGAG 360
AGCTTCAGGC CCCCTCTCCT TATCTTCTGC TAACCTCCAT TCTTACTCCT ACCCTTTCAT 420
CTCAGAATTT TCGCTTTGAT GTTTCCCACT TCCTTCCTAT GGTTACTTTA ACCGAAGTGA 480
GTCAGGTCTT ACTGAAAAAC TGACCACAGC CTGTCCGCTC CCAGCCTTCC CCAGACCAGG 540
GCTGCCCAGG CAGAGCGTGA GGGGGACTAG TGTTTACTCA GCTCATTTTT TTCCTCCTCT 600
CTCCTCTAAG TCACGGGGCT TTGAGTAGGG CTTCCCCAGC CACCGTGCCC CTCCCAGCAG 660
ACCGCAGTCA GAAGCCAATC TCACATTTGT CTGGTGGCTC AGAGAGGGGA CAGAAAGAGC 720
AGCAGCTTAT GTCCTTGGCT ATCCTCTCAA GTGGGCTAAT TTGCTTATTT TCAACTCTGT 780
TGGGTCCAGC CCTGTTGCCT CTGATCTCAG CTCAAAGAGG ATTTGGCGGG AGTTTTTGGT 840
TGTGATAACC AATAACAACC AACTATACGC ACTGCGAACA TCTCCTAGTG CCAGAAGCCC 900
TGTTAGCTCA TTATCTTAAT CCTCAGGATA ACCCAGGCAA TTTGTATTCA CCCTAAAAAC 960
TTCCCCTGGC CGGGTGTGGT GGCTCACGCC TGTAATCCCA GCAATTTGGG AGACTGAGGC 1020
AGGCGGATCA CTTGAGGCCA GGAGTTCCTA ACCAGCCTGG CCAACATGGT GAAACCCCAT 1080
CTGTACTAAA AATGCAAAAA ATTAGCCGGG CGTGGTGGCA CATGCCTGTA GTCCCAGCTA 1140
CTTGGGAGGC TGAGGCAGGA GAATCACTTG AACCTGGGAG GCGGAGGTTG CAGTGAGCTG 1200
AGATCATGCC ATTGCACTCC AGCCTGGAGA CAGGGCGAGA CTCCGTCTCG AAAAGCAACA 1260
ACAAAAACAA AAACAACCTC CAAAAAACCT TCCCCTGTTT ACCTTTCTAA TTTTGGTACC 1320
TACAGAATCT CCCCGTTAGC CTTGAAAATC AGCATGATCT TTAAGGATTT AGGAGCAAAT 1380
CTTTAAAGGA TTGAGTTGTG GGAAGACCAT 1410
|
