| Tag | Content |
|---|
EnhancerAtlas ID | HS177-11762 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr2:39334280-39335600 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:39334602-39334620 | CCTTCCTTCCTTACCTCT | - | 6.73 | | EWSR1-FLI1 | MA0149.1 | chr2:39334598-39334616 | AGTTCCTTCCTTCCTTAC | - | 6.75 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00320 | chr2:39333685-39335364 | Adipose_Nuclei | | SE_13832 | chr2:39334166-39335054 | CD34_Primary_RO01536 | | SE_18578 | chr2:39333693-39335802 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 39334288 | 39334718 | | chr2 | 39335032 | 39335193 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I039107 | chr2 | 39334341 | 39334542 |
|
Enhancer Sequence | GGAAAAACTG TACTTTATCC CGAATTAGGC AATTCATAGC CAGAGATGAC CCTAATTGAT 60
CATGAGAACG AGCCTCTCAG ATCTCTGACT ACAGGAAGGA TAATAGACTG AGTGCTGCAG 120
CAGCTGCACT CAAATCCATC ACTGTGTTTG TGTCGAGGCC AGTTTCTCAC TAGCTCCTCC 180
CAGTCACTGA CTGAGCATGG CAGGCCTGTT CCCGGGAGAC ACATCATTTT TCCAACAGGC 240
ACCTTTCACT CAAAGACTTT CTGAGGCCTT GCAAACTTTC CTTAGTATTG CACTACAGTC 300
TAAGACACTT TCACTCAAAG TTCCTTCCTT CCTTACCTCT CTTTTAACTT GGAGTCAGAC 360
TTTCATCAGT CTGACAACTC TCCCTGTCTC CTTCCTTTTC CCCCCTCACA AGCATTTCAC 420
CTAACAAATT TCTTATGTGC TTAATCCCAT CTTGGCATCT GCTTCTAAGA GGTCCTGGAC 480
TAATACAATG ACAAAGGCTC CCCTTGAAGC ATCACACTAA AAAGAAAAAA AAAAAAAAAA 540
AACCTAGCCA TTTTACATTA ACTATTTCTA AAATATAGTA TTTGCTTCCC TATTTGCTAA 600
AACAAAATAT ACTAAACATG ACTATTCCAA AATTCTGTAG GTACTAAGAA TATGAAGAGA 660
TTCACTCTAC TCAGGGGATG GAGTTGTAGT AGAAAGGCTT TGTGGAGGAG GTGGTGTTTG 720
AAATGTACTT TAGAGCCATC CTCAAAGCCT TGAGGCTATA CCTGCCTGTG ATTATCAAGG 780
ACAGTCCATC AAACAGGCCT TCCACGCTTG GATATCTGCC AAAGAGTAAA TCCCTCCTAT 840
CACAATTCTC TCACAGCCCT CTAATCTCTA GAATACTGAT GGTGCCTTAG TCTCCCTCCA 900
AACGTGATCC TCTCCCAATA TTCCCCCTTT CATCACCATC CCCACTTAGA CACCTCAGTC 960
AGAAACCTGG GAATCCTCTC ACTGCCCTGC TCAATTCAAT CACCAATCTG CCTCTAAATC 1020
TCTCTAATTA ATTTGTCCAC TTTTCTCCAT CCCCACAGCT ACTGCTCTAA TCAAAGCCAC 1080
CTATCATCCC TTCCATGAAC TACTGCAAAA TCTCCTCAAC TGGCTTTCCT GCCTACAGTT 1140
CAGTTCCCAT TTAATCCATG CTCCATACAG TCTACAGCAG TCCTTCAAAA TTCATGTGTG 1200
TCAGTTCCCT GCTTAAAACC CTGCAGTTGC TCCCCACTGC TGACAAGATA AAATGCAATA 1260
ATTTGATTCA CACGATCTGG CCCCCACTCC AGACTTCAGC TACTCAGAAC TCCAAAAATG 1320
|
