| Tag | Content |
|---|
EnhancerAtlas ID | HS118-11003 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:232278210-232279430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr2:232279393-232279405 | ACTAAAAATAGA | + | 6.27 | | MEF2B | MA0660.1 | chr2:232279393-232279405 | ACTAAAAATAGA | + | 6.32 | | MEF2C | MA0497.1 | chr2:232279391-232279406 | CTACTAAAAATAGAA | + | 6.57 | | NKX2-5 | MA0063.2 | chr2:232279335-232279345 | ACCACTTGAG | + | 6.02 | | POU2F2 | MA0507.1 | chr2:232278694-232278707 | AAATGCAAATGTA | - | 6.03 | | ZNF263 | MA0528.1 | chr2:232278650-232278671 | TCTCTCCCCTTTCCCTCCTTC | - | 7.38 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23390 | chr2:232276390-232279385 | Colon_Crypt_1 | | SE_25225 | chr2:232276440-232279498 | Colon_Crypt_3 | | SE_28347 | chr2:232273796-232280578 | Fetal_Intestine | | SE_61603 | chr2:232242399-232297770 | Toledo | | SE_68721 | chr2:232276462-232278618 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I231407 | chr2 | 232271526 | 232280793 |
|
Enhancer Sequence | ACCAGCAAGG AGATGTGTGG GCTCACAGAA GTGAAAGTAC AGGGATGCCT GCCTCAGGGG 60
CTGATGCAGG ACAGAAATAT AAAACAGCCA CTCCCCATAC TGGAGCTGCC TAGCTGGAAA 120
GGGGCAGGTT GAGATTGCTC TCAGGTGGCC TGACTGCAAA AGCTGCATGT TAGCCACCAC 180
TCAGACACGT GCTAGGGTCT GGAGGATGGA GGCAAGTCTG GAAACAGCTG CCTGTCCACC 240
ATGACTGCCT GCAATTTGTT AAGACCACCT GCAATTTGCT AAGCGCTGAT GGGGAGGCCA 300
GGCTCAGCTC AGATAGCTCA GCTCCCGCAG ACCTAGTCGA ATGTTTCTTG CTAGATTTTA 360
TGTATTTTTG TAACCAAATG CTCCCATTTT TTCTAAGAAA AACGGAATGA ATTACTTTTT 420
TTTTAATTAT TATTTTCTAT TCTCTCCCCT TTCCCTCCTT CCCGTTTCCT ACTCAGCCCT 480
TCAGAAATGC AAATGTAACC GTTCACCTCC CCCTAGACAT TCCCTTCAGG GTAATTCCCT 540
TCAGGGCAAT TTCTTCAACG GCTCCAAGAC AGATCTTTTC CTTGAGAGCT GACAGTCGAT 600
TTGCTGACAG TTGATTTCCA GACTGAAGCG TACCTGCCAC GGAACTTTTA CCTCCATGGG 660
GTGACCTTAG AACTTCTGCT CTGCAAACTG GAAGTGACCT TCATCCTCCA GGAGGGTATG 720
TCGAAAGCAT TCCCGCTTGG CCACTTTTAC AAGTTATTTC TGCCTGGGAA GGCACCAACT 780
CAATTATCCA GTAGATAAGA TACGGGGCAA CAGGGGAACG CCTGCCTTGC ATACTTGCTC 840
ACCCCCGACC TTATAAAAGT GTCCATGTTA CTGCTCCAAA GGTGAAGCAG CACATGTAAA 900
GGCAGGACGC GTTGTGTCCC TTCCCCAAGC TACCTTTGGA ATACATTCAC TTTTCTTACA 960
CCAGACCTCG CGCTTGTTCA TTGGACTCTG CATGCGATGA GCAACTAACC TGCTTTTCAG 1020
TTATGCTTTG GAGCCATGTT GTTTAGCACT TAGAAAATAG AGGTGGGTCT GGGCGCGGTG 1080
GCTCATGCCT ATAATCGCAG CATTTTGGGA GGCCGAGGTG GGTGGACCAC TTGAGGTCAG 1140
GAATTCAAGA CCAACCTGGC CAACTTGGTG AAACCCTGTC TCTACTAAAA ATAGAAAAAA 1200
TGAGCCCAGC ATGGTGGCAC 1220
|
