Tag | Content |
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EnhancerAtlas ID | HS078-01753 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr1:202002760-202004560 |
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 | Foxq1 | MA0040.1 | chr1:202003046-202003057 | AATAAACAATT | - | 6.02 | 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: 24 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:202003070-202004639 | Colon_Crypt_1 | SE_23723 | chr1:202003133-202004433 | 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 | CAAACCTGCA TGTTGTGCAC ATGTACCCTA TAACTTAAAG TATAATAATA ATAAAAAAAA 60 ACACAAAAAT AATTGTAACC CATTGCCCAC CCTAGCCCTG CCCGCCTTCC TATCTTCTTT 120 CTTGGTTTTA TTTTTCTCCA TAGCATTTAT CATGCTCAGA CACACAAAAT ATTTATCTAT 180 TTTTGCTGTT TGTAATTGTC TTTCTCCCCC CACTAAAATG AACACTCCGT GAGGGCATGG 240 CATTTTGCCT GCTTTGCTCA CAATGTGTAT CCCACTGAAG ACATCCAATA AACAATTTAT 300 CGAATAAATG AATGCATCTA CCTGATACCT CATCAAGAAA TTGATGACCA CTAATTATCA 360 TCTTTGAACC TCTGATTGGT GACCTCTGGC AAGGCTGAGG ACCTTTAGCT CTAATCAATG 420 GGCAAAAGGT TGACCTCTTT GCTACTGATT GGCTTTTCCT TTTCATTATA CCCTTGGGCT 480 GGATGGGGAA GCTGTGTGAA TCAACGCTTC ATAAGCCTTC CTCTCTGAGA ACTAGGGCTT 540 CCAAGGAATT GGATATGAAA AGGCAGAGAG GAAGGAGGAG GATATGAGAT GCCAGACGGG 600 GGAGGGTGGG GGGGACAGGT CCCAGAAGAG GTCAGCTGGG ACCCAGGCAG GATGGCATTG 660 TGGCTGCGGG TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT 720 GGGTAATCCG TGGTAAGTAC CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG 780 TTGATCCTCA CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA 840 GAAGCTGGCA CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG 900 GGGAATGGGG GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT 960 AAGGGTCTGT AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT 1020 CTACAGAGTC ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG 1080 TGGAGGAGCC CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC 1140 CCTGGGACCA GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT 1200 GCCCTCAGCT CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA 1260 GGTTCCCCAC CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG 1320 ACGGTGACGT CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC 1380 CTGGGGAGAC TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT 1440 GGAGGGCCTC AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA 1500 CATACCCTAG TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT 1560 CCTTGGCCAC TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC 1620 AGCATATATA AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT 1680 TTGCCTAAGC TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC 1740 TAAACTTAGA TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT 1800
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