Tag | Content |
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EnhancerAtlas ID | HS120-04591 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr3:57957580-57958980 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr3:57958904-57958915 | AAATCACAGCC | + | 6.02 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_23194 | chr3:57956577-57959307 | Colon_Crypt_1 | SE_23980 | chr3:57957440-57959195 | Colon_Crypt_2 | SE_26426 | chr3:57957184-57959281 | Duodenum_Smooth_Muscle | SE_27681 | chr3:57955209-57961457 | Fetal_Intestine | SE_28779 | chr3:57956485-57961614 | Fetal_Intestine_Large | SE_34631 | chr3:57952227-57967994 | HeLa | SE_38454 | chr3:57954542-57961940 | HUVEC | SE_50199 | chr3:57956484-57959322 | Sigmoid_Colon | SE_52474 | chr3:57956553-57960336 | Small_Intestine | SE_56605 | chr3:57957773-57959283 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I057966 | chr3 | 57952462 | 57961827 |
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Enhancer Sequence | AAGGGCCCAC ACGTGTGGCC ATTTACTATT ATATATGGCA CTTAAGGAAC AGCTCTGAGC 60 TCAATACATA GATCCTCATA AAACAATAAG ACCCTGAGGC AGTGGCCCAC GAGACACTGA 120 CTGTGCCATG TCAGTTGTGT TGTAGGTGTT CAGAGGAGAG AGTAAAGCTG GAACGACCCA 180 GGGAGGACAT GGTCTGGCCT TGGACCTTGA AGAGGAGGTG AGACTTGGAT TAGTGCATTG 240 GGAGGGGTGT GGTTTCAGGT GGGGACAAAG GTGTGGAAGT AGGGCTGGGT GGGGCCCCAC 300 TTAGAGGCGG TGTCTGGGGT AAAGTCAGGG GCAGGGAGGG CGGCTGGCCA GCTTCCAAGT 360 GGAATTGAGG CATAAAGCAG GGCTGAGGCC CAGGCCAGGA GCCGAGCACC TCCTTTTCCT 420 GTTAGCCTCA TTTCCCTTCC TCAGGGACCC ACAGAATAAG CTCTTAACTA GAAGCTATTG 480 TCCCTGCCCC CTCAAAATCC CAGTTTGGAG GCCCAAATGT CAAAGGGGAG CGATGGCTCT 540 CTGGGCCAGT GGCGTGGGGG TAAAATAATT TACCAAGACA GTTGTAGGCA GAAAAAGGCT 600 GATTTATTGG AGAAAGTAGA AAAATAGGTT GCAAGGAGAC AGGGCAGCCT GCATGAGAGA 660 TGCCGACTGC AAAGAAACAA AGGCTGGCTG GAGATTTTAT AGGACGGTGC TGACACTGTG 720 TGCTGAAGAG GGCTGTGCGC AGCACCACGA CGCCAAGCTT GCAGTGAGCT CACCTGCAGG 780 TGTCTGGTGG TAGCTGGGCA CAGGAAGATG GTGAGTTACT TGCGCAGGAG GGCTGTGTCC 840 TGGACCACAA AGAAAGGCAG ACTTGTAACT CATCTGCTTC TGCTTTTGCT TTCCCTGGTC 900 CCACCAGCCT GACTCCCTTT CCCTCATCAG GACTCCTCCA CACCAAGGAA ATAACAGGTC 960 CCCCTGCTCA GATTCAGCCT CGAGCCAGCA ACAAGGGGAG TCGGAGGAGG CCTTTAGCCT 1020 ATTTTATTGG TTTATTTTCT TCTCACAGCA AATATGCCCA GCCTGTGGCA GGCATCCAGG 1080 CACACCCAGT ACATGTTCCT GTCCTTCCTC CCCTTGCAGG TATGGAGTGG GACCCAGTCC 1140 CGACACAGAC TCACTGTCCC TCTAAAACCA CATCCACCCC CACCTCAGAA ACGGAAGTTT 1200 CACTGAAGGT TTCTTAGGAA TTTAAAAGGC AAGGTTCCTT CCCAGTTTAG CAAGACTTTC 1260 TGAAAAGCTC ACCTCCCATC CCAGGGACTT TTTTCCCTAG GGCCCCAGCT TCAGCCCTCC 1320 TCCCAAATCA CAGCCTCCTC TTTGCCTCTC CAGATGAATC CCAGTCTGTG GCCCACAGCC 1380 CTCACATTCT TAAACTAAGT 1400
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