Tag | Content |
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EnhancerAtlas ID | HS086-01186 |
Organism | Homo sapiens |
Tissue/cell | HEK293 |
Coordinate | chr1:202003530-202004710 |
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 | TCACATGTGG TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC 60 ATCTATGTAA GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG 120 TCCTTATTTG GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG 180 AGCCAGGACT AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG 240 TTCTCACCAT CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC 300 TCACACTAGG TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA 360 GCACCAGGGC CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG 420 TCAGGAATGT GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC 480 CCCGACCGCA GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC 540 TAGCTCAGTG ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT 600 TCACCTCTCC CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA 660 GCTTCATCCT GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC 720 TGCATGGTCA CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG 780 ACCGCCCCGT CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA 840 ATTTGTCTAC AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC 900 ATTTTCCATT TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA 960 CATTTCCATC TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT 1020 CCCAGTACCT TTTAGGGGGT TGAGGCGGGT GGATCATTTG AGGCCAGCAG TTCAAGACCA 1080 GCCTGGCCAA CATGATGAAA CCTCGTCTCT ACTAAAAAAT ACAAAAATTA GCTGGGTGTG 1140 GTGGCAGGCG TCTGTAATCT CAGCTACTCG GGAGGCTGAG 1180
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