Tag | Content |
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EnhancerAtlas ID | HS141-10701 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr2:128143300-128144270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr2:128144102-128144113 | TCAAGGTCAAA | + | 6.14 | RORA | MA0071.1 | chr2:128144101-128144111 | ATCAAGGTCA | + | 6.02 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_09644 | chr2:128141853-128148952 | CD14 | SE_10675 | chr2:128144112-128148979 | CD19_Primary | SE_11490 | chr2:128143043-128150313 | CD20 | SE_28345 | chr2:128144076-128147229 | Fetal_Intestine | SE_29146 | chr2:128143818-128147607 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GGGAAAGAGA AAATCAACCT GAAACCAACG CTGTAGGAAA TGCAGAGTAT CAAACATGAC 60 TTTATTTTAA TACAGCACCT GTTAGTTTAA CCCTTTGGTA CCAATAAAGT AAACTAGAAA 120 CAAAAGCTCC CCCTAAAACA TTGCTTATAA GACTCAGTCT CTAATGCAAT CCAATTATTT 180 AAGATAAGCC TTTAACAGCT AGTTTCTCAA AAGAGGCACA TGGATAACCA TTCTATAATG 240 ATATCATATA CAACATAATT CAATAAGATT CAACATGTTT ATATTTTAAC CAAACAACAA 300 ATCAATCTGT AAACCATCCA CATGTTAACT TTGTAATTTC ACCTTTTCTC CACAGAGACT 360 GCAAGACCAC AAATTTTCTT CAACTTGATA ATATACTAGG AAAATTACAG AGTAATATAA 420 CTGGGCATCA ATAGATTTGT TAAACATTTG CAATTATGCA TAGAGCTTCA ATTACTCAAA 480 GGAAATGTAT CGACTTTTTT TCAGTACAGA GCTCTGGCTC CTTATTTTTT CCTCTCACCA 540 TAGTTTTAAA AAATACAAAA CTCATGCTAA AATGAGAATT TTCAGTTAAC TTATAAACAC 600 TGACTAGTAG CACTCCATAC AAATGAAAAA GAATCACACC ATCAAACTTC CTACGATATT 660 CTACGCATTA AAATTTGACA TCGAACTAAA AAAGATTGCA TAAGACAACG AACAAATCAC 720 TAAATTGCCA CATAATCCAG CAACAAATTT TGCAACAAGG AAATCTCAAG CAAATAACCC 780 AACTGTGAGT TCCCTTTGGG CATCAAGGTC AAACTACAAA AGTAAATTTG TGACTTTTCA 840 AGATCTATGC AGTTTTACCA AATGTATTTA TTTTTTGTGA GAGAATAATT TTTTTCTGTC 900 CAGTACTAGT ACATAAAAAG TAAAGGTATC TGAAGCCATC TTTTAAATTT TTTTTAAAGC 960 CAAGAAAATG 970
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