| Tag | Content |
|---|
EnhancerAtlas ID | HS105-59577 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr4:6989290-6990500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr4:6990150-6990161 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr4:6990149-6990160 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr4:6990150-6990160 | TCAAGGTCAT | + | 6.02 | | IRF8 | MA0652.1 | chr4:6989954-6989968 | ACTTTCAGTTTCGT | - | 6.79 | | IRF9 | MA0653.1 | chr4:6989954-6989969 | ACTTTCAGTTTCGTG | - | 6.25 | | Nr5a2 | MA0505.1 | chr4:6990146-6990161 | GAGCTCAAGGTCATT | + | 6.51 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27343 | chr4:6987640-6990525 | Esophagus | | SE_27664 | chr4:6986645-6990188 | Fetal_Intestine | | SE_28549 | chr4:6986220-6990418 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTACTCTTT GTGTCTGTGT TTCCACGTAT TTTCTTCTGG TTCACGTTTA CTAGGACGAC 60
GAGAGACAGC GTGAGCGAGC ACGTCCTTTG AGTCCTCCTT ACCCTGTTTT CAGAGCCGGG 120
CCAGGCCCAG CAGCCCCCTT AGAGGTCAGA AGGGCCTCGC CTGCGATCCG ATGAGCCTTT 180
GTATGGAGAT GAGACTGCGC TCCGAGCTCT AGAGCCCAAT GAGGTGGTCA GGTTGCAACA 240
GCAACCGGGC GTGTTAAAAC CTAGTTCCTT TGAATATGTT TCATTCACCA GCCCGCATAT 300
TAACTTTTGA TGCTCTGGGA GGAATATGAC TATTAGAAAA GGACTCCTGA GAGTGCTTCC 360
CAGAATGCCA ACATTCCCAG TAACTTAGAG AACGCTTTCC AGGAGGGGAC TGCAGCTTGT 420
TAAAGAACCC AGGCCAGAGG AACCACTCAG ATGTTCTCAG TGGCTTTACT TACTGTGAGG 480
TCAGGCTTCA GGGGTTAGCC GGGGCTGCCT TTTGGAAGGT GGGACCTTTC TAAGACCTGT 540
GCAGGCCATT CTTCCCCCTC AAAATGGCAA AACAGCCCCT CCCAGATGCT AAACTGGGCT 600
CCCCCCTCCA AGACAATTGC TTTTACAAAT GGCCAAGTGT GAGACCAGCC GCGGTGTTGC 660
GGACACTTTC AGTTTCGTGC CCTTTTCCAC AAGCAACCCT CTTAGAGTGG AATGTTGTGA 720
AGAGTAATTT CATAGTATAT AGTGACAGTC ATACTCCTAT CATTTCTGGG CACCTGCTTT 780
GGCTCTGCAG CTTATGCTGG TTCTCATTTA ATCTTCAAGT GTAACAGATG AGGAAACAGG 840
CTTGTGGATG GAGGAGGAGC TCAAGGTCAT TCTGCTGGTG GTGCTGGCTC AGACCAGGCC 900
TGCCGCTGTC CCCCAGCGCT TCCCTGGGTC CTCAGCCTGT GCAGATGTGG TGGCCGTGCT 960
GTCACAGCAT TAGTTCAAGT CAGTCTTTTG ATAGGTACCA CTCGGATGGC CAGCCTGCCT 1020
TGGCAGCTTT ATTCCAGGCG CGCTCCCAAA TCCTCAGGTT ATTTTCACTG GTGAATCTTG 1080
ATACTGCAGA CAGCGGGGTC GGAGATTTAA GCACAGGATT TGACTGATGA CCCTTTCCTC 1140
TTCTAGGTAA AATAGATTTC CAGGGAGCCA GAGGCTCCTT CCTGGAAGTC AGGGGGCTTC 1200
CAGTAGCAGG 1210
|
