| Tag | Content |
|---|
EnhancerAtlas ID | HS051-24770 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr7:29628160-29629030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr7:29628287-29628305 | GAGAGGAAGGAAGGATGT | + | 6.15 | | EWSR1-FLI1 | MA0149.1 | chr7:29628486-29628504 | CCTCTCTTCCTTCTTTCC | - | 6.6 | | EWSR1-FLI1 | MA0149.1 | chr7:29628283-29628301 | GGAGGAGAGGAAGGAAGG | + | 7.26 | | IRF1 | MA0050.2 | chr7:29628387-29628408 | AAGAAAAAAATGAAACAAAAA | - | 6.4 | | ZNF263 | MA0528.1 | chr7:29628365-29628386 | AGAGGAGAAGAAAGAAGAGAG | + | 6.29 | | ZNF263 | MA0528.1 | chr7:29628493-29628514 | TCCTTCTTTCCCTCAGCCTCC | - | 6 | | ZNF263 | MA0528.1 | chr7:29628280-29628301 | AGAGGAGGAGAGGAAGGAAGG | + | 8.14 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28371 | chr7:29627455-29629251 | Fetal_Intestine | | SE_28611 | chr7:29627290-29629293 | 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 |
| GH07I029587 | chr7 | 29627597 | 29629129 |
|
Enhancer Sequence | AAGCCACCAG TTAGTGATCA TTTGTTTTGG CAGCCACAGG AAACAAATAC ATCATCTTTA 60
GCTCCTGTGG TCCCTCCCTA TCACATCAAG TGAATACACG TTACTCTGCT GACTGTTGTG 120
AGAGGAGGAG AGGAAGGAAG GATGTACAGA AAGCATAAGA GAAGAGGGAA AAGATGGGAC 180
TGGAGTGGGG TAGAGAATGT CAAAGAGAGG AGAAGAAAGA AGAGAGGAAG AAAAAAATGA 240
AACAAAAACG AGCAATGAGG TAAAAATGGG TTGTTGTCTG CTCAGACCCT TTGAGCTTCT 300
CTTTGTCCTC ATCGGTCCAC ACACAGCCTC TCTTCCTTCT TTCCCTCAGC CTCCCCCAGC 360
CCCCCATGCA CCTGCCACAC TAAGCAAGTT CATTTTTGTG CTGTTCTGAC TTCCTGTCCC 420
ATCCCACGTT CTGCTTTCCA ATCTGCAGGC GCCAGTGAGA GGGGAAGAAG CCTGAGCAGA 480
GGGTCTTGCT CACCCAGAAA GTTCCGCTCC ACATCCCATC AATCACCCTA AAGAGAAGCC 540
AGGGGACCCG GGCCACTCGC CAATGCAGGG TCTCCTGGGC TCAGGCAGAT ACCCGAAACT 600
TGCCACCTCA AGCACCCACT TGGAATGCTT CTGCTGTCAC ATCACTCTGC TCTATCTGCC 660
ACCCACAACC CAAGTAAGTT AAACAGAGGA AGTGGCCCAG AACTGCCAAG TGTGCCCTCA 720
GAAAAATCTC CAAAGGCAGA GGTCAGGAGG CTGTAATCAT TTTGGGGATT ATCTTCCGGG 780
CTTAAGTTGG GGCTTTAAGC TTCTCTGTGC TGCCTCTAGT GGTCACTGGA AGGAATGCTC 840
CTCTGAAGGA CGCAAGGGCT GCTGGAGCAA 870
|
