| Tag | Content |
|---|
EnhancerAtlas ID | HS056-08562 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr2:39702970-39704670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:39703062-39703080 | CATTCCTTCCTTCCTGTC | - | 7.16 | | EWSR1-FLI1 | MA0149.1 | chr2:39703054-39703072 | TCTTCCTTCATTCCTTCC | - | 8.52 | | EWSR1-FLI1 | MA0149.1 | chr2:39703058-39703076 | CCTTCATTCCTTCCTTCC | - | 9.09 | | IRF1 | MA0050.2 | chr2:39703838-39703859 | AACTGCTTTCACTTTTTCTTC | + | 7.27 | | MEF2C | MA0497.1 | chr2:39702994-39703009 | TTCTATTTTTGGCAG | - | 6.85 | | SPIC | MA0687.1 | chr2:39703853-39703867 | TTCTTCCCCTTTTG | - | 6.21 | | ZNF263 | MA0528.1 | chr2:39703042-39703063 | TGTTCCTTCTTCTCTTCCTTC | - | 6.02 | | ZNF263 | MA0528.1 | chr2:39703054-39703075 | TCTTCCTTCATTCCTTCCTTC | - | 6.2 |
|
| | 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 |
| GH02I039476 | chr2 | 39703261 | 39704473 |
|
Enhancer Sequence | GTGAATGCTT CTCCATGTTG TGGTTTCTAT TTTTGGCAGT CTTTCTTATT TCTCTCCCTC 60
TCTCCTTTTC TCTGTTCCTT CTTCTCTTCC TTCATTCCTT CCTTCCTGTC CCCCTAGGCT 120
TAACCTTCCT GGTCTCATAG TTTTGCCGTT ACCTACTTTC TGGGCCTCCC AGGCCTAGAC 180
CTCGGTTTTA TCCTATAGTA TTGTAGATCC AGTTCCTTCT CTAGGGTCAA ATTCCGTCTT 240
TAAGACTATG CCTGGTTCTT CCATGTCCCT AGGTATACAG ATGTTTACAA GCCTGTAGCC 300
CTAGGCAATT CCTTTCAAGG GGGTAGCCTT ATCCCAGCCC TTGATTTCAT GTGAGTCTTC 360
TGCCTCACAT GGGTTATTTA GTTCTTAGTA CCCTGTATGA GTCTTGCCCC TGGATGCCTC 420
TGTTTGCTGT TGGCAGAATT GAGCTGGTCT ACATCTTCAG GCTACTTACC ATATTGTTTC 480
TGTTCCATTT CTGGGCTATG GAGATGTTTT TAAGTGTGAA AATGCCTTAC ATTTTTCCCA 540
TTTTATATTA AATCTATTAT CACTATCATT TTGGATTGGC GTGGTCCTCA AAGCCCCATC 600
TTGACTAGAA ATCAACTAGC ATTTGCTTCT CTGCAGTTCG TAATCTAGCT TCCTCTCTCA 660
CCTTTCTCTT GGCAATTGCC CTCTCTGAAG TCACTGCTGT TGTTTCCGAG TCACTGAATG 720
AAACCGTTTT TCCTTCAGCC CCCATTTTCC TTCACTCCTC TGCAGCATCC AGCAGTGTTG 780
ACTGCTCTTC CTTTTACCTC TCTCCTGTTG GCTGTTAGGA TGCTCTGCTG TCCCGGATCA 840
CTACCTCTTC TGATGCTTCC AGTTTTTAAA CTGCTTTCAC TTTTTCTTCC CCTTTTGTAA 900
CTGTGGATGT CCCACAAGGC CAAGTCCTTG GTGCTCTGGT TTTACCCTCT ATTTCAGCTA 960
ATTTTGCTTA TTCTCATCTT TGGTCATTGC TAAGTCCCTA TCTGTTCACC AGGGCTTCCC 1020
CCTCCCCTGA GTTCTAAGCT ACAGATCTGC TTGTGACACG TTCCACTTGA TGCCCTGCTG 1080
TTCCATCAAA TTTCCTCCCC TTTAATCCTC CCAAATGCCA TTACAGATAT CATTATTCTT 1140
AGATGGAGTC TTGCTCCGTT GCCCAGGCTG GAGTATAGTG GTGTGATCTC GGCTCACTGC 1200
AACCTTCACC TCCTGTGTTC AAGTGATTCT CCTGCTTCAG CCTCCTGAGT AGCTGGGATT 1260
ACAGGCATGC ACCACCACAC CAGAGTAATT TTTGTATTTT TTGTGGAGAT GGGGTTTCAC 1320
CATGTTGGCC AGGCTGGTCT CAAACTCCTG ACCTCAAGTG ATCCTCCCAC CTCAGCCTCC 1380
CAAAGTGCTG TGATTACAGA AGTGAGCCAC CATGCCCAGC CTGTTATAGA TATCATCTTT 1440
CCCTTAGTTT CTAAGGCTCA GAATCATACC CTTCCTTGAT TCCTCATATT TTCTCCAGAG 1500
TCAGTTAATT ATACATCCTA TCCATCCTCT TTCCTGTCAT TTCCTCTTTT TGCCATTGCA 1560
CGGCTCACAC ACCTGCTATG GTCCCTTGTT ATTTCTTCTT TTGGACCATT TTGGTATTCT 1620
TCCAGAGAAG CAGGACAGTT AAATGTGGCA ATATTTGGAC TCATTTGTGT TCAAAATTTG 1680
TGATATGGAT TCTTCCCACA 1700
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