Tag | Content |
---|
EnhancerAtlas ID | HS176-29089 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:70638860-70640150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr4:70639349-70639360 | AAAGATAAGAA | - | 6.62 | SRF | MA0083.3 | chr4:70639533-70639549 | TTACCCTATATGGTCT | + | 6.07 | TBP | MA0108.2 | chr4:70639215-70639230 | CTATAAAAGGGAGGG | + | 6.66 | mix-a | MA0621.1 | chr4:70638889-70638900 | ACTAATTAATT | - | 6.62 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28395 | chr4:70638171-70643186 | Fetal_Intestine | SE_29144 | chr4:70638189-70643162 | Fetal_Intestine_Large |
|
| 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 |
GH04I069772 | chr4 | 70638231 | 70643094 |
|
Enhancer Sequence | CCAACAATTG CCCAGTTCAT GGAAAGCCCA CTAATTAATT TACTTGGGAT AATTTTACTT 60 ATTTTGCTTT ACTGTTGTGG AATATATTGC TGTTTTAGTC TTTGCATAGG TATTCAGGAC 120 AATGTTGAAT GTTGTATTAT ATTGAAAACT TATTAATCTT CCAGTAATCA CCTTTTGTCA 180 GAATTCGGAG TTATATATGG CACTAGCCAT ACCAACACTT TCTGACTGAG CTCCTCTCTA 240 TTCTAAACAC AAGAGACCCT CATGGTTAGG CAGGAATATC ATCACCTTTA TTCAGCAGAA 300 AAAGTTACAG AAGATGGATC TTCATCCCTC TGCTCTCTTA GGATAAAGGG TTCTCCTATA 360 AAAGGGAGGG GGTAAATGTC AGAGGCATGT GAACTGGAGC AACTCCAGCT TAAATAAGAG 420 CTAGGTAAAA TGAGACTGAT ACCTACCAGG CTGCATTCCC AGACAGTTAA GGCATTCTAA 480 CTTACAGGAA AAGATAAGAA GTTGGCACAA GACACAGTTC ATAAAGACCT TGCTGATAAA 540 CAGGTTGCAG TAAAGAAGCC GGCTAAAACT CACCAAAGCC AAGATGGTGA CGAGAGTGAC 600 CTCTGGTTAT CCTCACTGCT ATGCTCCTAC CAGTGCTATG ACAGTTTACA AATGCCGTGG 660 CAATGTCAGG ATGTTACCCT ATATGGTCTG AAAATGTGAG GCATGAATAA TCCACCCCTT 720 GTTCAGCATA TCATCAAGAA ATAACTACAA AAATGAAAAA TGGGCAACCA GCAGCCCCCA 780 GGGCTGCTCT GGCTGTGGAG TAGCCATTCT TTTATTCCTT CACTTTCTTT TTTTAAAAAA 840 ACTTTTCTTT TTTTTCTGTT TTTTTGGTCA TCCAGGCTGG AGTGTAGTGG TATGATCTCA 900 GCTCACAGCA AACTCTGTCT CCTGGGTTCA AGCGATTCTC CTGCCTCAAC CTCCCAAGTA 960 ACAGGATTAC AAGCAAGCAC CACCACGCTT GGATAATTTT TTGTGTTTCT AGTAGAGATA 1020 GGATTTCACC ATGTTGGCCA GGCTGGTCTC AAACTCCTGA CCTCAAGTGA GCCACCCTCC 1080 TCGGCCTCTC AAAGTGCTGG GATTAGAGGT GTGAGCCACC AAAGCCCAGC CTCCTTTACT 1140 TTATTAATAA ACTTGCTTTT GCTTTGTGCT GTGGACTAGG CCTGAATTCT TTCTTGTGTG 1200 AGAGCCAAGA ACCCTCTCTT GGGATCTGGA TTGGGACCCC TTTTCTGTAA CACTGGTACT 1260 ATAGACTAAG ACTGATCCTA GCCTTTAGAA 1290
|