| Tag | Content |
|---|
EnhancerAtlas ID | HS187-13968 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr2:136549580-136551030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr2:136550941-136550953 | GCAATCACTGCA | + | 6.14 | | ZEB1 | MA0103.3 | chr2:136550022-136550033 | GGGCAGGTGGG | - | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 136549992 | 136550234 | | chr2 | 136549800 | 136550600 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I135791 | chr2 | 136548983 | 136550615 |
|
Enhancer Sequence | TTTGAAAGAA GCAGAATGCT ACTGCAAACT CCATGAGACA GCTGCAAAAC TGTGAGTTCC 60
CAAAGTGTGA GAAGGGGAAA GTCTGCCTCT GAACACACAT CCTCTCTGGG GACCTGAACA 120
TCCAGATCAT AGGAGAAGGA TTTAACCTTA CCTAGAGCGC AAGTGGATTT AGGGAGCCAA 180
GTGAAATGTA AAAGTAGAAG AAGCAGTGGG AAGAGCCCTG TAGCCACTCC CTGTCCCCAG 240
CTTGAGCCCA GGGAAGCCAT TCCTGACTTT ATCCTACAGG GGTCCTTGTA GAAGGAAGCC 300
AGTGGAATTA GGGAGGGGCA GGATTAAGGA AGCTTCTAGC TCAACTTATT AATTTCAACT 360
AGAAGCATGA ATTTTCCTGA GCAGAATCTT GGGGGCAAAC AAGAAGTGCA GATAAAAGCA 420
CAGAAGCCAC AGCCAACAGT GTGGGCAGGT GGGGAGGGGC AAGGCCTGAA AGCCCTGTTT 480
GCTTTCTCAG AGAGAAGGCT TGTGGCCTGG GGTGAGATCT CTGCCCTGCG CACTGTTGGC 540
AGGGCACAGC AGGAGTGAGA CTGGCCTTGC TGGCTGCATG GGAGCTAGGT GAGGCTTGTG 600
ACTGCCAGCT TTCCCAACTT CCCTAGCAAC CTGTATGACA CAGCAGAGGA AGCCATAATA 660
CCCCTGGGAA CAGAACTCCA CTGGCCTGAG AACCAGCCCC CTATTCCCCC ACAGTGGCCA 720
CAGCAAGCCT CACCCGAGGA GAGTCTGAGC TCAGATATGC CTAATGCTGC CCCAACCTGA 780
TGGTCTTTCT CTACCTTTGC TGGTAGCTGA AGACAAAAGA CATAAACTCT TGGGAGCTCT 840
ATGGCCCCGC CCATAACCTG AGAAACCCAA ATACCCTGGC CAACGTAGGG CAACCTTGTA 900
ATCCCCCTTC TACTACCGCA GCTGGTGGCA GTGGAAGGGG AAAGCACCTC AAAAGTGCCA 960
CCTCCTCTCT TGAAAGTGCC ACCTCCTGGC TGGAGACCAA CCAACTCACG CCATTATAGC 1020
AACTCATAAC AGAAGAACCC TGCTCCAAAG AAAGAGAAAA CAACAACTAA TTCCACTGCC 1080
TGCAACATCC TGGCTAACCA GAGGTCCTGA GTCTGTCCAC ATGACAACTT CACTGCTCGC 1140
ATAACCAGCG TTTGAGAAAA CCAGTGCACG AAAGAAAACT ACAACCAAGG ACCCTCACAG 1200
AATCCACTTA AGTCCCCTGC CACCTGCACT GGAGCAGGTG CTGGTATCCA TGGCTGGGAG 1260
ACCTGAAGAC AGATCACATC ACAGGACTCT TTGCAGACAT TCCTCAGCAC CAGTTCAGAT 1320
CCCAGTAATT CTGCTGGGTG GATAGACCCA GAAGGGCAAT GGCAATCACT GCAGTCTGGC 1380
TCTCAGGAAG CCCCATCCTT AGGGAAAGGG GGTGAGCACC ACATCAAGGG ATCACCCTGT 1440
GGGACAAAAG 1450
|
