| Tag | Content |
|---|
EnhancerAtlas ID | HS018-10696 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr18:74920430-74921760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr18:74921026-74921047 | TTTCACTTTCTCTTTCCTCTG | + | 6.67 | | IRF1 | MA0050.2 | chr18:74921020-74921041 | TTCCAGTTTCACTTTCTCTTT | + | 9.66 | | IRF2 | MA0051.1 | chr18:74921025-74921043 | GTTTCACTTTCTCTTTCC | - | 6.79 | | NFAT5 | MA0606.1 | chr18:74921565-74921575 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr18:74921565-74921575 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr18:74921565-74921575 | ATTTTCCATT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 74920800 | 74921580 | | chr18 | 74921028 | 74921148 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I077206 | chr18 | 74918749 | 74922095 |
|
Enhancer Sequence | CTTTCTTTAC ATACATTGAG AACATCAGAC AGCATTATCA TTTTTGCTTC CAACCATGGA 60
ACATAATTTA GAAAACTCAA GAGGAGAAGG AGTCTATTTA TTTACCCATA TTTTTTACTT 120
TTGCTGTTGT TCTCACTTTC TTCCCAATAT TCCAATATTG CTTCTTTTAT AATTTCCCTT 180
CTGTTTAGGA AACTTCCTCG AGCCATGCTT TGAGTAACCC TGCTGATGGC AGATTCTCTT 240
AGTGCTCCTT CACTGGAGAA TATCTCTATT TATACCCGTC CATGAGGGAC ATTTTCCCTG 300
CCATAGACTT TTGGTTGACT GGCCTTTTCT CTTGGTATTT GAGACGCTTG CTACTTCCTT 360
TTGGGTTCCA TGGTTTCAAA CGGAAAATTT GCACGTCCTA CAAGCAATGT GTTTCTCTCT 420
GGCTACTTTG CAGCTATTTT TCTTTGTCTT TAGTTTTTCA GACCTTTGAT TATGATGTAT 480
CTTGGTATAA ATTTCTTTGG GTTTACCACA TTTGGAATTT TCTCAGATCC TTGAATCTTT 540
AGTATATTTC ACTAAACTTG GGAAGTTTAC AGCCATTTAA AAAATATACC TTCCAGTTTC 600
ACTTTCTCTT TCCTCTGAGG ATGACACAGG CTCCTGAGAG TCTGTTCTTT CTCCTCAGCC 660
CACTTCCTCA ATGCTGCTCT GAGTTGGTGA CTTCTGGCCC TCGTCCAGTC TTTTGTCCTC 720
TCGCTGTCCT GGTTGAGTCC ACGCATTGAG GTTTTAGGTT TGTTTGTCTT TTGGTTATTG 780
TGTTTTCTTG CTTTATAATT TCTTTTTTTT TTTTTCAGAC CGAGTCTCAC TCTGTCACCC 840
AGCTGGAGTG AGGTGGCATG ATCTCTGCTC ACTGCAACCT CTGGCTCCTG GGTTCAAGTG 900
ATTCTCCTCT CTCAGCCTCT CGAGTAGCTG GGACTACAAG TGCCCACCAT CGTGCCAGGC 960
TAATTTTTGT ATTTTTAGTT GAGGTGGGGT TTCACCATGT TGGTCAGGCT GGTCTCGACC 1020
TCCTGACCTC AGGTGATCCA CCTGCCTTGG CCTCCCAAAG TGCTGGGATT ACAGGCGTAA 1080
GCCACCATGC CCGGCCTCCT TTGGTTCTTC TTTATTCTTT TGCTAAAATT GTCTAATTTT 1140
CCATTTATTC CACGGGAATT CATACATGCT GAAGTGTATT TATGATGGTT ATGTGAAGAT 1200
CCTGCTCAGC TAATGATAGC CTCTGACTCA TCTCCGTGTT GTCATCCATC GGTTTATTTC 1260
TCCTTCCAGT TGTGATTATC CTAGTTCTTG GTATGCTGAG TGACTTTGGA TCGGAGCCCG 1320
TACATTTAGG 1330
|
