Tag | Content |
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EnhancerAtlas ID | HS179-02935 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:202003380-202004570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | + | 6.14 | CREB1 | MA0018.3 | chr1:202004082-202004094 | GGTGACGTCAGC | - | 6.14 | NFAT5 | MA0606.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr1:202004430-202004440 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:202003070-202004639 | Colon_Crypt_1 | SE_23723 | chr1:202003133-202004433 | Colon_Crypt_2 | SE_23723 | chr1:202004446-202004634 | Colon_Crypt_2 | SE_24689 | chr1:202003019-202005179 | Colon_Crypt_3 | SE_25977 | chr1:202003098-202005224 | Duodenum_Smooth_Muscle | SE_26730 | chr1:202003201-202004852 | Esophagus | SE_27624 | chr1:202002753-202007729 | Fetal_Intestine | SE_28545 | chr1:202002635-202005490 | Fetal_Intestine_Large | SE_31432 | chr1:202003030-202004833 | Gastric | SE_33417 | chr1:202002752-202008344 | H2171 | SE_33792 | chr1:202002877-202005297 | HCC1954 | SE_34304 | chr1:202003057-202005125 | HCT-116 | SE_34741 | chr1:202002989-202005297 | HeLa | SE_41626 | chr1:202003359-202004353 | LNCaP | SE_43434 | chr1:202002760-202004009 | MCF-7 | SE_43434 | chr1:202004034-202004676 | MCF-7 | SE_50066 | chr1:202002922-202004883 | Sigmoid_Colon | SE_52354 | chr1:202003018-202004869 | Small_Intestine | SE_56834 | chr1:202002917-202004651 | VACO_400 | SE_57376 | chr1:202003233-202004124 | VACO_503 | SE_57376 | chr1:202004143-202004423 | VACO_503 | SE_57945 | chr1:202003251-202004112 | VACO_9m | SE_57945 | chr1:202004146-202004634 | VACO_9m | SE_65333 | chr1:202002930-202005541 | Pancreatic_islets | SE_67013 | chr1:202002752-202008344 | H2171 |
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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 |
GH01I202033 | chr1 | 202002815 | 202007566 |
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Enhancer Sequence | CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG TGGCTGCGGG TGCCAGAGTC 60 AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT GGGTAATCCG TGGTAAGTAC 120 CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA CAGCCATCTC 180 TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA CTTAAAAGCA 240 CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG GTGGAAGGCG 300 CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT AGCCTCCTAA 360 ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC ACTCCCCTCC 420 ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC CTCACAGATC 480 TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA GCTGGTGGTT 540 TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT CAAGAGAACC 600 CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC CCACCCGTGG 660 CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT CAGCCCTGCA 720 GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC TGGATTACCT 780 CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC AAAGGCCCGT 840 CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG TATGCGGGTT 900 CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA 960 TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA AATATACATA 1020 TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC TTGGGTGGCT 1080 TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA TGTATGTTTA 1140 GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT 1190
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