| Tag | Content |
|---|
EnhancerAtlas ID | HS050-04143 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:151944920-151946030 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEOX2 | MA0706.1 | chr1:151945407-151945417 | GTTAATTACT | - | 6.02 | | NKX2-3 | MA0672.1 | chr1:151945587-151945597 | ACCACTTGAA | + | 6.02 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_27992 | chr1:151944503-151946921 | Fetal_Intestine | | SE_28908 | chr1:151944506-151951024 | Fetal_Intestine_Large | | SE_33866 | chr1:151943574-151946166 | HCC1954 | | SE_34778 | chr1:151944627-151946042 | HeLa | | SE_47215 | chr1:151938610-151969225 | Panc1 | | SE_50609 | chr1:151945020-151945804 | Sigmoid_Colon | | SE_52876 | chr1:151944902-151945719 | Small_Intestine | | SE_56104 | chr1:151944501-151945780 | u87 | | SE_67706 | chr1:151944501-151945780 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 151945068 | 151945221 | | chr1 | 151945012 | 151945852 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I151971 | chr1 | 151944026 | 151946837 |
|
Enhancer Sequence | ATCTGGGTGT CTCACGTTGG GTTTAAACTT ATGAATAGGT ATAAAAGAAT AAGTAGAAAT 60
GAGAAAATAC TGCTTTGACT CCTCACCTTA ATCTGAAATT AGAATGAAAT TGTTCATGAA 120
TTGTGTAGTC ACAGCTGCAT TAAGATTAGA TGCCCCAGAG CCATATTTAT TGGCTTGGAA 180
ATATTATCTT CATTTGCTGG CTTCCATAAG CAACAAAAGA ATGTCACCAT TCACGTTTTG 240
CTCTGCATGA CTTGGCGATT CCTTCGCATG CATATATGAG TGTTAATTTC TTCATCACAC 300
ATTTGCAGAG CCCCTAGTAC ATCTTGGATG TTATAGCAGG CTCTGAAAGC ACAGCAGTGG 360
AAAGACTTGG TCCCTGTACT TACAGTATAA TAGGGACAGA CGTATGAGCA AGTAATTGTA 420
GTATAATGTG ACGAGTGTGA TAATTAATGC ATGCACAAAG AAAAGTGGTG GCCCCAAGGA 480
GAAAATAGTT AATTACTGTT GTGTGTGGGG GTGTGGATTT AAAGAAGTAG TCACAGAGGA 540
AGATGTCACC AGTTCTCAGC AGTGGCACAT AAATGAAAGG CAATTAAGTA GCAGATGTGA 600
GTTCTTTCAC ACTTTCTTGT CCCTGCTTCT TACTCCCTCC CTCTTGCTGA CTGGAAGTCT 660
CTGAGTCACC ACTTGAAGGA GAGCGGCCAG ACTCACTGTA CTTTAATGTG CTGTTTGACT 720
CAGCAGTTAA CCTCCTGTGA TACGGCCTGT CTGTTCTGTT GCCAAATTAC ATAAATTTGT 780
TATTAGACTT TGAGGACTTA CAGCTAAGTC ATTAAGGCTA ACTCTAAATC AGTTCATGAA 840
TTATAAATTA TTTTGGCAGC AACATTATCC ATAGACCTAC ATAACTTCTG TCATTTTTGT 900
TGAAAGCTAT CTCCATGATT TCTTTTTTTT TCTTTTTGAG ACAGGGTCTC GCTCTGTTAC 960
CCAGGCTGGA GTGCAGTGGT GCGATCTCGG CTCACTGCAG GCTTGACCCC CTGGGCTCAA 1020
GCTATCCTTC TGCCTCAGCC TCCCAAGTAG CTGAAACTAC ATGCACAAGC CACCATACCT 1080
GGCTAATTTT TAAATTTTTT GGAGAGATGA 1110
|
