| Tag | Content |
|---|
EnhancerAtlas ID | HS182-13235 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr2:219732000-219733380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr2:219732800-219732814 | GGTCCCTTGGGATT | - | 6.44 | | KLF13 | MA0657.1 | chr2:219732724-219732742 | CTGCCACGCCCCTTCTGG | + | 6.89 | | KLF14 | MA0740.1 | chr2:219732725-219732739 | TGCCACGCCCCTTC | + | 6.39 | | SP2 | MA0516.2 | chr2:219732028-219732045 | AAGTGGGTGGGGCTGAA | - | 6.41 | | ZNF263 | MA0528.1 | chr2:219733076-219733097 | GGAGGAGGAGGGAGAGGAGAA | + | 10.16 | | ZNF263 | MA0528.1 | chr2:219733172-219733193 | TGAGGAGGAGGGACTGGGGAA | + | 6.34 | | ZNF263 | MA0528.1 | chr2:219733073-219733094 | AAGGGAGGAGGAGGGAGAGGA | + | 7.47 | | ZNF263 | MA0528.1 | chr2:219733079-219733100 | GGAGGAGGGAGAGGAGAAGGA | + | 9.8 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGTCTTGCTC ATCTGCATAA CGAGGGTGAA GTGGGTGGGG CTGAACTGGG TGATCTCTGA 60
CATTGTTCTT GGCCCTCTGA CTCAAGAGAT GGAAAGGTAG GTTAGGCCAG AAACCTAGGA 120
CATCCAGGGC TTAGGTCTAC ACATATTGCC AATAGGGACT GGCTGGCCCC TGATACCACC 180
TCCCTAGGCA ATTGATCCTA CCAACCATGG TCCTTGGTAG AGAGACCTTG GCGCAGGCCA 240
AGCCGGTTAG AATGACCATC CATTGCCTTG TCCCTTCTTG TCCGCATACT GATTTCTTTT 300
AGGGCTAGCC TCATTTTTTT CTATGCCCAG GAATGGCTGT TTGATGAGGA TCCCAGATCC 360
TATATATTGT GTATTCCCTA CTACCACTGT GCTTCAGGCC CCAAAACATG CAAATTCTCC 420
CAAAGGAGCA CATCTTCTCT GGGCTGATCC TAGGCCAATG CTGACCCAAA GGCCTGAAAA 480
GCAGAGTTCA CTCCCTAAGG AAGCATAAAG CGAGGAAGGT GAAAGGTGAG TGGGGATGGG 540
GGAGTTATTA CTTGATGTGT TGTCAAAAGC CAAAGTTATA GGGGGTACGT GAGTCTCTCA 600
TGCTAACTCC TCAGTTTTTC TGAAGCCCAC AAAGGGGAAT GACTTGATCA GAGTGGCTCA 660
GCCCACACAG AGTTGACAGA AACCAGAGAT CGGAAGCGAA GCTTGGTGTT TTGCCCAATG 720
CCCCCTGCCA CGCCCCTTCT GGAGTTTCAT TTCCTATGTA TTTAGGATGG GAGCAAGGAC 780
AGGAGGGCAG GGAACAAACT GGTCCCTTGG GATTCTAGCT GCTACTACTG CCCATCCCTC 840
CCCCTGACCA GCTTGTAAAC AAGTCTAGTT CCCAGGCAGC CAGCCAGCCT GGGGAGCCAG 900
ACCCAGACCA GGAACTGGCT CTGGGGCAGT CCCCCAGCCC CAGCCCTACC TCCTGAAAGT 960
CCCTGGCCTC CATACTCCTC GTGATTCTCC CGTCTCTAGT CCCTGCGAAA CAGAGAAGGT 1020
CAAGAGGTTT TTGTCTTTCT GTCTTGCTCA TCTCCACTCC CTCCTGCCTT CTTAAGGGAG 1080
GAGGAGGGAG AGGAGAAGGA TGGGGCAGAG TAACCTTGGG AAGATAAGGC CAGGCAACCC 1140
TGGGAAACTA GGGAGTTAGC AGAGGGCAGG GTTGAGGAGG AGGGACTGGG GAACTTAGAA 1200
GTAAGGGAAG TGGGGGTGGG GAAGATGAGC TTGCAGAGCC CCCGACTCAC AGGTGGAGCC 1260
CCAGACATAA GGGGCTGGAC GACTGCAGAG AGGACTCATT CCCTGCCTGA TTCCCAGTGG 1320
GGGAAAAGAG CATGTTTGAG GAAATGAATT AGGAGTCATG AAATAAGATG TGGACAGGGG 1380
|
| |
|
|
|
