Tag | Content |
---|
EnhancerAtlas ID | HS182-02574 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr10:70987370-70988670 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr10:70988625-70988643 | GAAAGAAAGAAAGGAAGA | + | 6.22 | Nr5a2 | MA0505.1 | chr10:70988098-70988113 | AACTTCAAGGTCAGC | + | 7.13 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27984 | chr10:70979065-70991295 | Fetal_Intestine | SE_28850 | chr10:70987227-70988524 | Fetal_Intestine_Large | SE_53047 | chr10:70986422-70990508 | Small_Intestine |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr10 | 70988000 | 70988600 | chr10 | 70988586 | 70988668 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH10I069227 | chr10 | 70987399 | 70991090 |
|
Enhancer Sequence | GCATCTCCAT GTTCTTCCCT GGTGAGTATC AACGTGGCTT TTCCGTCTCA GCGTAGTGGT 60 CCCTGCCTCC ATCTAGGAAG TATCCCTGTG CTGGGCTGGG TGCTTGTCAG GGCACTTGTC 120 ACTTTGCTGT GTCCCCACTC TGAGTCTCCA CCAAATTAAC CACTCACTCC GTGGGTCCAA 180 GGTCTTACCA CAGTGTTCCC AGCACCTAGT GTAGCACTGG GAATGAGTAA TGGGAGCAAG 240 AATGATGTAG TGGAAATCAC ATTCAATGAT AATTCAACAA ACCTGGGTCT GAGGCCCAGC 300 TCTGTCACTC TCAGTGACCT GAGGCAAGTG TTTAGCCTCA GTTTGCCCAG CTGTAGAATG 360 AGAAATGGCC TATGTATCTG TTTCCTATGG CTGCTGTGAT GTATTACTAC AATCACAGTG 420 GCTGAAAACA ATCGAATATA TTCTCTGACA GTTCTGGTGG ACGGAAGTTT GCAGTGGGTC 480 TCACTGGGCC AAAATTCAGG TGTCGGCAGG GCTGCGTTCC TTCTGGAAGC TTGAGGGGAG 540 AATCTGTTTC CTTAACTTTT CCAGTTTCGA GAGGCCACCT GCATCCTTGA GGCATGCCCC 600 TTTCTGTTCT CAAAGCCAGC AGTGTAGCCT CTTCAGGTCC CTCTCTGACC TGACCTTCTG 660 CCTCCTTTCA ACATTTAAAG ATCCTGTGAT CACGTTAGTC ATGCTTAGAT AATCCAGGAT 720 AATCTCCCAA CTTCAAGGTC AGCTGATGAG CAATTTTGAT CCCATCTGCA ACCTTAATTC 780 CCCTTTGCCT TGCACCCTCA GATATTCACA GGATCTGGGG ATTAGGATGT GAGCATCTTT 840 GTTGGGGGTG GGGGACATTA TTTTGCCTAC AATGGCCTAG AAATCTGTAG ATAGGATCTA 900 TGAGGTCCCA TCCAACTCTT CCATTCTCAG CCTCTGAATG AAGCTGTAAG AGGGAAAAGG 960 GCTGCTACTG GCCTGGAGTG GTGGCTCACG CCTGTAATCC CAGAACTTTG GGAGGCCGAG 1020 GGGGGCAGAT CACTTGAGGT CAGATGCTCG AGACCAGCCT GGCCAACATG GTGAAACTCC 1080 ACCTCTACTA AAAATACAAC AATTAGCCAG GTGTGATGGC ATGCACCTGT AATCCCAGCT 1140 ACTCGGGAGG CTGAGGCAGG AGAATCACTT GAACCTGCAA GGCAGAGGTT GCAGTGAGCC 1200 GAGATTGCGC CACTGCACTC CAGCCTGGGT GACAGAGCGA GACGCCATCA AAAAAGAAAG 1260 AAAGAAAGGA AGAAGAAAGA AAGAAAGAAA GAGAGAGAAA 1300
|