| Tag | Content |
|---|
EnhancerAtlas ID | HS018-01507 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr1:158615670-158616750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr1:158616222-158616238 | GTGCCTTCTAGGAACT | + | 6.11 | | BCL6B | MA0731.1 | chr1:158616223-158616240 | TGCCTTCTAGGAACTCA | + | 7.18 | | HOXA13 | MA0650.2 | chr1:158616172-158616183 | GTTTTATTGGG | - | 6.62 | | IRF1 | MA0050.2 | chr1:158616332-158616353 | AAACTGAAAGCAAAAGTATCA | - | 6.56 | | IRF1 | MA0050.2 | chr1:158616326-158616347 | AAAACAAAACTGAAAGCAAAA | - | 8.18 | | IRF9 | MA0653.1 | chr1:158616328-158616343 | AACAAAACTGAAAGC | + | 6.01 | | Nkx3-2 | MA0122.3 | chr1:158615793-158615806 | TTTAAGTGGTTTC | - | 6.52 | | REL | MA0101.1 | chr1:158616518-158616528 | GGGGATTTCC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 158616370 | 158616536 | | chr1 | 158616442 | 158616596 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I158646 | chr1 | 158615991 | 158616710 |
|
Enhancer Sequence | CCTTAGAAAA GGTAATTAAT CTGCCTATGT GGTATAACTA AAAGCAGACA TCTTCAATAA 60
AACCTAGACC TCTGGAATCC TGGACTGTTA TATATTTCAT TACTTCTGTT GGTTACTGTT 120
CCTTTTAAGT GGTTTCTAGG GTTTGAAGAT ACATCTTATT ACAGAGTCTC AAAGAAATCA 180
TGTCTTTCCT CTTACTTTTA TTCTCAAGTG AATCTAGCAC ATATTTTGGC CAACATACAC 240
ATACACACAC AGGCCTCCAC ACTGTTGATT AAATCAAGGT CTATTTCCCT ACCCTTTTAG 300
TAGTCAGGAA GTTAGACGAG CAAAACTAAG GTCTATCTTC TTAAAAGGCA AATTTTAACT 360
ATGCATTAAC TTTAAAGCAT ATATGGTGTA TAAATTAAGC ATCTCATAAA GAATGTCATT 420
ACTCTTGTTT GCTCAACAGG AACCCTTAGC TCTAGGAAAG AGAGGTCTCT TCTTTTGTAA 480
ATTTATTTAT TCAAGCAACT AAGTTTTATT GGGTGCTTAC TAAGTACCAA ACATTGTGAA 540
AAAGGCATAT CTGTGCCTTC TAGGAACTCA TACTTTAGGT TAAGAATGGA TAAAAACAAA 600
ACAAAACAAA ACAAAAAACA AACAAAAAAC AGAGCATAGG CACTAATAGC AATTAAAAAA 660
CAAAACTGAA AGCAAAAGTA TCATATGGAG TAAAATAAGA TGTTAATGTT GCTCAGGGGT 720
GGGAACACTA CTCTGAAATA CTGAGGAGTA CAGCTTCATA AAGGGAAGGA AGCACCATTG 780
GAATGGGTGT GGGTGCTATT TATTTAAACT GTGTCAAAAA CTATAGCTTT CCAGTGCTGA 840
ACTGGGGAGG GGATTTCCAA GAGGAACTAC AGTCATTTGC CAAAATTTGC CTCCTTTTTT 900
CTTGAAAAGC ATTGCATTGA GAGCTACAAC TTCCTGGACC CTCTACTCTA ATGCTCCTCT 960
CAGCTGACTG ATGCGATAGA GCCAAACGTG GGAACTGTTC CACAAAGTAT ATGTTTGAGA 1020
GGTGAATTTT GGATTGTGAT AATGTCTAGA CTTTAGTAAG ATATTCACAG TTCTCTGGAA 1080
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