| Tag | Content |
|---|
EnhancerAtlas ID | HS060-28889 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:2866100-2867260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr6:2866596-2866611 | AATTAATCAATAACA | + | 6.08 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_28080 | chr6:2865882-2867415 | Fetal_Intestine | | SE_28996 | chr6:2865858-2867021 | Fetal_Intestine_Large | | SE_38162 | chr6:2865399-2867166 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 2866705 | 2867019 | | chr6 | 2866631 | 2866750 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I002864 | chr6 | 2865041 | 2867315 |
|
Enhancer Sequence | TAGTTCAACT ATAGCCAATC ACTAATCAAT GTTATTTCTG TAAACCAATG AGAATTCTTA 60
ACCAACAATG TTGGTAATTG CCTCCTCTCC TGATTCATCC TTTGTTCTCT GGGCACTTCC 120
CAAGACAACT TGGAAGTGTT TCCCAAGCAG CTGTTCTCAA CCCTGACCCA AATAAACTCT 180
CATATTAATT TTGCCTCAGC TTCTTCCTGT CAGTCGACAA CTCCTAACTA GCTATTTTCA 240
TCCCTTTTCA AGCTTCCTAA GAGGTTACTT TCATTTAGGT TCGTGATATA ATAAAAAATA 300
TATCTGGTGT TTATCCCCAG TTCCCGGCAC AGAGCTCCTA AAACCCTTGG AATTTCCTGA 360
GTAATGCGAG TGTGTTTTGC TATTCAAAAT GAGCCGCTTT AGCTACACCT GAGCTTATGC 420
TGATGAGGCG GCTCTTGGTG ATCCCCTGGG GAGGGAAGAA GGGCTGGGAA TTGAGTTCAG 480
CCACCAATGG CCAGTGAATT AATCAATAAC ACCTATGTAA TGGAACCTCC ATAAAAATCA 540
AAAAGACCAG GTTGAGGGAG CATGTGGGTT AATGAACAGA CAGGTGCTGA GAGGGTGGAG 600
TGTCTAGAGA GGGAATGGAA GCTCTCTGCA CGCACCCCCG ACCCCCCTTA ACTTGCTCTC 660
TGCATCTCTT CCACTGGTTG TTTCTGCCTT TATAATAAAC TGGTGATAAT AATAAAGTGC 720
TTTCTTGAGT TCTGTGAGTC ATTCTAGTAA ATTATTAAGC CTGAGGGAGG TTATGGGAAT 780
CCCCAAATTT GTACTTGGCC GGGCAGCAGT GTGAAGAGCC TGGGCACCCC ATTTGTGACA 840
GGTGTCTGAA GAGGGGGTAG TCTTGGGGGC TGAGCCCTCT AACTGGACGT TAAGTACTGT 900
CAGAATTGAA TTGAATTGTT GGACACCCAG TTGGTGTCAA AGAACTGATT GGTGTGAGGA 960
AAAAAACCTC TTAAAGGTCT TTACTCCCAC TTACTGGTAG TGTTGCTAAG TTCATAATGC 1020
CTTTTTCTTA TCACTCATGG CTTCATTAGG CTTGACTTAC TGGTCTTACT TGCCTAGATT 1080
GGTCTTGAAC TCCTGGGCTC AAGCCATCTT CCTGCCTTGG CCTCCCAAAG TGCTGGGATT 1140
GCGGGTGTAA GCTACCATGC 1160
|
