| Tag | Content |
|---|
EnhancerAtlas ID | HS060-20721 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:216675670-216677200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:216676977-216676998 | AACATCTTTCACTTTCAGCTT | + | 6.27 | | RARA(var.2) | MA0730.1 | chr2:216675801-216675818 | TGACATTTTGGTGACCC | - | 6 | | SPI1 | MA0080.4 | chr2:216676528-216676542 | GAAAAGAGGAAGTG | + | 6.92 |
|
| | 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 |
| GH02I215811 | chr2 | 216676124 | 216677096 |
|
Enhancer Sequence | AAGATAAACT AATTCGACAC TTCAGAACAC TCACTTCCAT TCTTTGAAAT CTGTGCTTCC 60
TAGGTGGCTA TCTTCAGACT TTGCATTTGA ACACTTTAAA CTAGATTTTG ACCCTTTTGA 120
TTATTTTAGG ATGACATTTT GGTGACCCAG ATGGGACCCA AAGCAAGCCG CCAGTGATCC 180
CCACCATTTC ACCAACAACA GTCAGGGCAC TGGTATTAGC ATGAATGACT TTTGTTCACT 240
CGACCTCACT AGAGCCAGGA GGAGTCTCTG GTGAGGTTCC TCTTCAAGTT CAAATCTCCC 300
TGATTTTTGT TGATATTCAG ACCTTATTCA AGCCACCTAA TTCCACGCTC AATAGAGCTG 360
GAATTAAAGC TCTGCTTTTC AGGTAAGGTT TTGGGTTTTG TTCTCTAGAG ATTCTGCTCT 420
TTGCAGGTTT TGTTTTGTTT ATTTTGTGTT TTGTTTTGTT TTTATAGACA GAGTCTTGCT 480
TTTTTTTATA GACAGAGTCT TGCTCTGTTG CACAGGCTGG AGTGCAGTGG TGCACTCATG 540
GCTCACCGCA GCCTCAAACT CCTAGGCTCA AAGAATCCTC CCACCTCATC CTCAGGAGAA 600
GCTGGGACTG TAGGTGCAGG GCCACCATGC CTGGCTAACT TACTTTCTGT AGAGACAGGG 660
TCTCATTATG TTGCCCAGGC TCATCTCCAA TACTTAGCCT CAAGTGATCC TCTCAAAGTG 720
CTGGGATTAC AGGCATGAGC TACTGTGCCT GTCCTATAGA TTTAGGTTAA CAGTTGTTTG 780
TTGAACTATG CATTAGAGTT TGTGCAGCCT TTGCTCTCAT TCGCACTATG GTCAGGAAAG 840
GAAACCATTT CTCTCTCTGA AAAGAGGAAG TGAATTTTTT TGTGGTTTAA GCAAAGTTTG 900
TAATTAAAAA AAAAAAAAAC TGGCTAAACT TGGAAGCTGG GTTCATTTGA CATATCTAAA 960
GTCCCTTCTG AGTGGCCAAA GCCAGGGAAA AGCTTTTAAT CAGAATGAAG ATAAATCCTG 1020
AAGATAAGGG ACACTATTCT TCCTGGACAA AATGTACCTT AGGCAACTAG GTTCCTGTGG 1080
GAGTGTTTGA GCTCATTGCT TGTGATGTGC AATGGTCCCA TAGGCAATCC TCAAAGAAGA 1140
ACACAGGGGG AATCTTGCTT AACCCAGGGG GCCCCATGAA AGGCTGCTCT CCCTGTGCCT 1200
TAAGCACCCA GGACTCATGG GTTTTGCCAA GATGTGTAAG AGGGGAGAAG CAACTCGTAG 1260
GTGACACCTT GAGGAGTAAT CCTCATTGGG CAGCACACCA CATCCAAAAC ATCTTTCACT 1320
TTCAGCTTAA AAAGAACTTA ATTTATGGGC AGTTATCTAT GTAAAACCAC ATCTTCCTTC 1380
TGAAAGGAGA GATCAACCTA TGGAAACTCC AGTTGGATTC CTAGGCAATA CTTATGGGGC 1440
CACCTCCTGT CAATATCTAG AGAAATAGTC TTAACCCGTG AAGACACCAA ACTACAATGG 1500
CCAAAATGAG ATACTTTTGA AATACCTAAA 1530
|
