| Tag | Content |
|---|
EnhancerAtlas ID | HS050-16032 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr12:56480440-56481360 |
Target genes | | Number: 41 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX1 | MA0002.2 | chr12:56480609-56480620 | AAACCACAGAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_23624 | chr12:56479942-56480774 | Colon_Crypt_1 | | SE_23624 | chr12:56480794-56482434 | Colon_Crypt_1 | | SE_31786 | chr12:56479792-56482740 | Gastric | | SE_48005 | chr12:56481254-56481754 | Pancreas | | SE_50964 | chr12:56479836-56482109 | Sigmoid_Colon |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I056085 | chr12 | 56479501 | 56480786 | | GH12I056087 | chr12 | 56480978 | 56481818 |
|
Enhancer Sequence | GTAAGTGGCC GTGATCAAGA TTGCTCCCCA GTCCCACCAA ACCAGAGTGA CTCCCTTCTT 60
TCCATCATCC TTACATTCCT GATCTGAACC CGCCTCCCCA GTGAACAAAC ACCTCAGGTC 120
CCTGACTCAG CAGCCCACCA GGGCAGACCA TTCCAGTCTC CTGGAATCTA AACCACAGAG 180
GAGGTGTTTC AAGAAAAGGA GCAGGCCGAG CATGGTGGCT CATGCCTATA ATCCTGGCAC 240
TTTGGGAAGC CAAGGTGGGA GGATCGCTTG AGCCCAGGAG TCCAAGACCA GCCTGAGTAA 300
CATAGCAAAA AATCTACAAA AAATTAAAAA AATCAGACAG GCGTAGTGGC TCGCACCTGT 360
AATCCCGGCT ACTCAGGAGG CTGAGGCAGA GGATTGCTTG AGCCCAGGAG GCTGCAGCTG 420
CAGTGAGCTG TGATTGTGCC ATTGTACTCT AGCCTGGGCA ACAGAGTGAG ACCCTGTCTC 480
AAAAAAAAAA AAAAAAAATC CCTGAGTACT AAGCAGGGAA GCCAGATCTT TAGACTCCAC 540
ATCTGTTACT CGTTCCACTA GAATATACTC CCATTTCCTT GGAGCCCACC TTCCCCTGAC 600
CATTCACATG CATATATTCC TGCATATATT CAGTTTGCCC AGGAGGAACT AAGTTCCTGG 660
GTTGGGACTA GGACTAAGGT TGGCATTTGC CCCAGTCCCT CCCCTTCAGC TGCCCAGTGG 720
GTGGTGTGGA GGCGTGGCCG CGCCCCTTGT TGACAGGTCC ACTTGAGCCC AGCCCTGCTC 780
TCCAAGGGCA GGGAGGGACA CAGCCCTGGC TTTTTGCTTC CCGGGATTGA GGTGCCTGTG 840
TACTGACATC ATACCCCGTT GATTAAAACA AGCCTTTCTT AGCCCTGATG GCCCCTTGTG 900
TTGCCTTCCT TCCCAACCAG 920
|
