| Tag | Content |
|---|
EnhancerAtlas ID | HS095-15385 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr19:46379540-46380870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SP2 | MA0516.2 | chr19:46379910-46379927 | GTCACCCCCGCCCCCTG | + | 6.05 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23551 | chr19:46379389-46382979 | Colon_Crypt_1 | | SE_24599 | chr19:46379448-46380697 | Colon_Crypt_2 | | SE_24599 | chr19:46380733-46382349 | Colon_Crypt_2 | | SE_35762 | chr19:46376029-46383004 | HepG2 | | SE_47895 | chr19:46379418-46382977 | Pancreas | | SE_65443 | chr19:46378331-46381375 | Pancreatic_islets |
|
| | 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 |
| GH19I045875 | chr19 | 46378522 | 46383519 |
|
Enhancer Sequence | TCACCCTCTT TCTGTGCCTT TATCTGTGTT TCTTGGTTTG AGTTGCTGGT GCTGTCTGTG 60
TGTGTCTGTC TCTCCTATGG CTCACCTCAT GCTCTCTCTC TCTCTCCCCC CTCGCTCACC 120
CGGCCCCCGC CTTTTCTCTC TACTGCTCTG ACTTCCCTCC TCCCTCCACC TGGGTCTCTG 180
GGTTTCTCCC TCCTTCTCTC AGAGTGACTC TTTCCTGGGG TCCGTCTCCC CCCACTCCTT 240
TCCTGGATCT CTGGTCTCTC TTTCTCTGGC CTCCATCCCT CTCCCAGCTC TCTGGGTTTC 300
CGCCTCTACC TGCCACCTCG CAGGCCAGGC CCTCTATTCC TGTCGCTGCG CCCCGCCTTG 360
CCGGCTGCGT GTCACCCCCG CCCCCTGCCG CGCTGGCTCC CCGTCCGTCC CACCAGCCTT 420
GCTGTCCTGG GCAGGCCGGG GAATTCCTCC CGGTTCCTGG AAAAAACAAC TGGGGCCGAG 480
AGAAAGGCCC TCAGTCTCCC CAGGCACCCG CCCCCCTCCC TCGGGCCTGG GGGTCTCTCC 540
CGGAGTCGGC CAGCCCGAGG CAGGAAGCCC TGCGGTTTCT GGCTTCTCCC AGGCGGCCTC 600
CGGATCTGGC CCCCGCCCCC CGGCCAACAG CCCAAATATT ATTCCGCGGG AGGAGTCGGT 660
GGTGGCGGGA GGAGGCCCAG GCTGAAAGAG GCTTTCAGGG CGGCCAGGCC TGGGGCTTCC 720
TGTCCCCAGG CTCGGGCCTC AGGCCGCCCC AGTGGGGACC TCAGGTGGCC GGAGGGGCGG 780
GGTGTTGTTG TAGGGTCCTC GGGGGAGGGT GGGGCCATCC GTCGGGGTGT CTGGTGGCCA 840
CCAGCTCTGC TGGCGTGGGC AGGTGTGACC CCCACCCCAG GGACAGCCGG CTGATGTCCA 900
GCGTGGAAAA GTACCACGGT CAGACATGGG ACGCATGGAC AGACACGGGA CGCCACGAAT 960
CAGGGATGTG GGGTGGCCAT GGGGACACAG GCGGCCCTGG GCTGTGGGCC TAAGGTGACA 1020
TGGTCCAGGG GAGGGGCCTG TGGGTTGGAG CAGAGGCCGG GGCAGGGTCG CAGCTGTGGG 1080
CAGAGGGCTG TCAGCATTAG GAGGTACCAG ATGATGATGA TGATGATGGT GATGATGGTG 1140
ATGATGATAA TTAAAAGATC CTAGGGCTTC CCATGAGTCA GGGATTGTGT TAGCACCTTA 1200
CAGAACTGAT GGGCTCCATC TCTCCCGCTC CCCCCAACTT TACTGTTGAA TGAAACTGAG 1260
GCACAGAGAG GTGAAGTAAC TTGCACAGAT AATGAGTGGG GTGCTAGGGC ATGAACCCAG 1320
GCAGTCTGGG 1330
|
