Tag | Content |
---|
EnhancerAtlas ID | HS045-01382 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr1:39612920-39614090 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:39613157-39613175 | CCTTCTTTCCCTTCTTTC | - | 6.17 | EWSR1-FLI1 | MA0149.1 | chr1:39613061-39613079 | CTTTCCTTCCTTCCCTTT | - | 6.23 | EWSR1-FLI1 | MA0149.1 | chr1:39612980-39612998 | TCTTTTTTCCTTCCTTCC | - | 6.79 | EWSR1-FLI1 | MA0149.1 | chr1:39613153-39613171 | CCTTCCTTCTTTCCCTTC | - | 6.84 | EWSR1-FLI1 | MA0149.1 | chr1:39612923-39612941 | TTTTCCTTCCTTCCTTCT | - | 7.52 | EWSR1-FLI1 | MA0149.1 | chr1:39613145-39613163 | CCTCCCTTCCTTCCTTCT | - | 7.79 | EWSR1-FLI1 | MA0149.1 | chr1:39612988-39613006 | CCTTCCTTCCTTCCTTTT | - | 7.95 | EWSR1-FLI1 | MA0149.1 | chr1:39612984-39613002 | TTTTCCTTCCTTCCTTCC | - | 9.07 | EWSR1-FLI1 | MA0149.1 | chr1:39613057-39613075 | CCTTCTTTCCTTCCTTCC | - | 9.09 | EWSR1-FLI1 | MA0149.1 | chr1:39613149-39613167 | CCTTCCTTCCTTCTTTCC | - | 9.47 | POU4F2 | MA0683.1 | chr1:39614062-39614078 | TTCATAAAATATTCAT | - | 6.08 | SPI1 | MA0080.4 | chr1:39612973-39612987 | TTCTTCCTCTTTTT | - | 6.14 | SPIC | MA0687.1 | chr1:39612973-39612987 | TTCTTCCTCTTTTT | - | 7.01 | ZNF263 | MA0528.1 | chr1:39613038-39613059 | TTCTCTTTCCTTTCCTTCCCC | - | 6.05 | ZNF263 | MA0528.1 | chr1:39613132-39613153 | TCCTCTTTTTTCCCCTCCCTT | - | 6.12 | ZNF263 | MA0528.1 | chr1:39613144-39613165 | CCCTCCCTTCCTTCCTTCTTT | - | 6.27 | ZNF263 | MA0528.1 | chr1:39612996-39613017 | CCTTCCTTTTCTTTTTCCTTC | - | 6.29 | ZNF263 | MA0528.1 | chr1:39613170-39613191 | CTTTCTTTCTTTTCCTCCTTT | - | 6.41 | ZNF263 | MA0528.1 | chr1:39613053-39613074 | TTCCCCTTCTTTCCTTCCTTC | - | 6.65 | ZNF263 | MA0528.1 | chr1:39613141-39613162 | TTCCCCTCCCTTCCTTCCTTC | - | 7.1 |
|
| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_37973 | chr1:39612688-39614232 | HUVEC |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 39613773 | 39613853 | chr1 | 39613140 | 39613893 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I039147 | chr1 | 39612689 | 39614232 |
|
Enhancer Sequence | CTCTTTTCCT TCCTTCCTTC TCTTTTCTTT TTCCTTCTCT TTTCTCTTTC CTTTTCTTCC 60 TCTTTTTTCC TTCCTTCCTT CCTTTTCTTT TTCCTTCTCT TTTCATTTTC CTTCTCTTTT 120 CTCTTTCCTT TCCTTCCCCT TCTTTCCTTC CTTCCCTTTT CTTTTTCCTT CTCTTTTCCC 180 TTTCCTTTCC TTTCTTTCCT CTTTCTTTTC TTTCCTCTTT TTTCCCCTCC CTTCCTTCCT 240 TCTTTCCCTT CTTTCTTTCT TTTCCTCCTT TCTTTTCCTT CTTTCTTCTT CAACAGGGTC 300 TTGCTCTGTT GCCCAGGCTG GAGTACAGTG GCACAATCAT AGCTCACTGC AACCTGAACA 360 TCCCAGGCTC AAGCTCTCCT CCTGCCTCAC CCCTCATGTA GCTGGGCCTA CAGGCACACA 420 CAACCAAGGC TGGTCTCGAA CTCCTGGCCT CAAGCAGTCC TTCTGCCTTG GCCCCTCAAA 480 GTGCTGGGAT TATAAGCATG AGCCACCCCA CTTGGCCCTA TTTATTTTCC ACATCTGATT 540 GGACACTAAG TTCTGTTTGT CTAGCTGAAA AATATCTCAA CAGATATTGT TTCCTGGCTA 600 GACTCACTGC CCTATTTTAG ACCCTCGTCT TCTTTGATTT ATGCCAGTGG TCATGCCACA 660 TTTCCTCTTA AAAACTGATG ATCAGTTTCA CCCCTTGTTT ATGTTGTTTT CTATGCCTTG 720 AATGATCTTT TTACTTTTTC TGCCTCACAA ATGCTTGTTC ATACTGTAAT CTTTTGTCCC 780 AACTCAAAAC TTAATAGATT TTAATGGTGT TCCTGCTTCT TTCCTTCTAC CCCAACCAGT 840 AAAAAATTTC ACTTACCTTT TCATCTGAGT TCTTATGGTA GGATGTACAT CCTTTGTGAT 900 AGTATTTATC ATCTTATTTT ACAGTTTTCT GTTTAATTGT CAGCCTCCCC TAGACCATGA 960 GTTCAGTGAC TGCAGGCTGT ACTTTCTTCA TCTTTGTTTT TTGGTGCCAT AACAATTTGT 1020 AGAATTGTTG GGCTGTATAT AGAGTTCCTG CTTTCTCCAG ATAAAGAATG TTTAGAAAAA 1080 TCTGAAAGAG TTATGCTACT GTTGGATATT GGTTGTGGCA GAATCTCCCC TCCCCTTTTT 1140 ACTTCATAAA ATATTCATGT TTGTTGTAGG 1170
|