Tag | Content |
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EnhancerAtlas ID | HS095-02630 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:202003430-202004860 |
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 | TGCCAGAGTC AGCCTGCCTG GGTTAAGGTC CTCAGTCAGC CTTGACTGCT GGGTAATCCG 60 TGGTAAGTAC CCACTGCTCC TGCCTCAGCT TCCCCACCTC TCACATGTGG TTGATCCTCA 120 CAGCCATCTC TTGGGGTTGT TCTGAAGATG AAATGAGATC ATCTATGTAA GAAGCTGGCA 180 CTTAAAAGCA CAGAGAGGGC ACCAAGGAAC GTATGGTCTG TCCTTATTTG GGGAATGGGG 240 GTGGAAGGCG CCCAGCAGGG CATGGGGCGT GGTATGGCAG AGCCAGGACT AAGGGTCTGT 300 AGCCTCCTAA ATCAGGGCTT TCTCCGCAGG ATTTCCCATG TTCTCACCAT CTACAGAGTC 360 ACTCCCCTCC ACCCTGCTGC CCCGTTCCAC CAAGTGGCCC TCACACTAGG TGGAGGAGCC 420 CTCACAGATC TCTTTCCTTC AGCCTGCCGT TCTTTCTGCA GCACCAGGGC CCTGGGACCA 480 GCTGGTGGTT TCCACCAGAG CAGCCTCGGG GTGAATTTAG TCAGGAATGT GCCCTCAGCT 540 CAAGAGAACC CTCCCCAACC TTCCACTCCC CATACCCACC CCCGACCGCA GGTTCCCCAC 600 CCACCCGTGG CCTGGCCAGC AGCAACCTCC ACTAGCTCGC TAGCTCAGTG ACGGTGACGT 660 CAGCCCTGCA GTGCAGGCTG GGCTGGTTTA CCCGCAAGTT TCACCTCTCC CTGGGGAGAC 720 TGGATTACCT CACCCTGGGA GCAGAGTGAA TGATTAACCA GCTTCATCCT GGAGGGCCTC 780 AAAGGCCCGT CCTGGGGTGT AGGCCTACAG GGCAAGGGGC TGCATGGTCA CATACCCTAG 840 TATGCGGGTT CACATACCCC AGCCGGGGCT GGGGTATGTG ACCGCCCCGT CCTTGGCCAC 900 TGCCCTCTTA TCTGCATCAC TGCTCACAAG TGTCATAAAA ATTTGTCTAC AGCATATATA 960 AATATACATA TGACGTGGAA GGCTTCCGAT GGCAAATAAC ATTTTCCATT TTGCCTAAGC 1020 TTGGGTGGCT TTTTATTCAT CTATTGTTGT TTTAAGTACA CATTTCCATC TAAACTTAGA 1080 TGTATGTTTA GGCTGGCCGC GGTGGCTCAT TGCCTGTAAT CCCAGTACCT TTTAGGGGGT 1140 TGAGGCGGGT GGATCATTTG AGGCCAGCAG TTCAAGACCA GCCTGGCCAA CATGATGAAA 1200 CCTCGTCTCT ACTAAAAAAT ACAAAAATTA GCTGGGTGTG GTGGCAGGCG TCTGTAATCT 1260 CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CACTTGAACC TGGGAGGCGG AGGCTGCAGT 1320 GAGCTGAGAT TGCACCATTG CACTCCAGCC TGGGCAACAG AGTGACATTC TGTCTCAAAA 1380 ACAAAAACAA AAACAAAACA AAAAAAATAA ACTTAGATGT ATATTTAAAA 1430
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