| Tag | Content |
|---|
EnhancerAtlas ID | HS030-02159 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:206939190-206940570 |
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 | ACTTGTGAAC CCTGAAAATT TAAGACAGGT CTCAGTTAAT TTAGAAAGTT TATTTTGCCA 60
AGGTTGAGGA CATGTGCCCG TGACACAGCT TTGTCACACA GCCTCAGGAA GTTCTGATGA 120
CATGTGCCCA AGGTGGTTGG GGCACAGTTT GGTTTTATAC ATTTTAGGGA GACATGAGAC 180
ATCAATCAAT ATATGTAAGA AGTACATTGG TTCCATCCAG AAAGATGGGG ACAACTCAAA 240
GCAGGGAAGG GGCTTCCAGG TCACAGGTAG GTAAGAGACA AATGGTTGCA TTCTTTTGAG 300
TTTCTGATTC TTTTCCAAAG GAGGCTATCA GATATGCATC TATCTCAGTG AACAGAGGGA 360
TGACTTTGAA TAGAATGGGA GGCAGGTTTG CCCTGAGTAG TTCCCAGCTT GACTTTTCCC 420
TTTAGCTTGG TGATTTTGAG GCCCCAAGAT TTTCCTTTCA CAGACTCAGG ATGTCTTCTT 480
CAGTTCAGGA TGGACAGCCT CAGAGTAGAG AGCTTCAGGC CCCCTCTCCT TATCTTCTGC 540
TAACCTCCAT TCTTACTCCT ACCCTTTCAT CTCAGAATTT TCGCTTTGAT GTTTCCCACT 600
TCCTTCCTAT GGTTACTTTA ACCGAAGTGA GTCAGGTCTT ACTGAAAAAC TGACCACAGC 660
CTGTCCGCTC CCAGCCTTCC CCAGACCAGG GCTGCCCAGG CAGAGCGTGA GGGGGACTAG 720
TGTTTACTCA GCTCATTTTT TTCCTCCTCT CTCCTCTAAG TCACGGGGCT TTGAGTAGGG 780
CTTCCCCAGC CACCGTGCCC CTCCCAGCAG ACCGCAGTCA GAAGCCAATC TCACATTTGT 840
CTGGTGGCTC AGAGAGGGGA CAGAAAGAGC AGCAGCTTAT GTCCTTGGCT ATCCTCTCAA 900
GTGGGCTAAT TTGCTTATTT TCAACTCTGT TGGGTCCAGC CCTGTTGCCT CTGATCTCAG 960
CTCAAAGAGG ATTTGGCGGG AGTTTTTGGT TGTGATAACC AATAACAACC AACTATACGC 1020
ACTGCGAACA TCTCCTAGTG CCAGAAGCCC TGTTAGCTCA TTATCTTAAT CCTCAGGATA 1080
ACCCAGGCAA TTTGTATTCA CCCTAAAAAC TTCCCCTGGC CGGGTGTGGT GGCTCACGCC 1140
TGTAATCCCA GCAATTTGGG AGACTGAGGC AGGCGGATCA CTTGAGGCCA GGAGTTCCTA 1200
ACCAGCCTGG CCAACATGGT GAAACCCCAT CTGTACTAAA AATGCAAAAA ATTAGCCGGG 1260
CGTGGTGGCA CATGCCTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GAATCACTTG 1320
AACCTGGGAG GCGGAGGTTG CAGTGAGCTG AGATCATGCC ATTGCACTCC AGCCTGGAGA 1380
|
