Tag | Content |
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EnhancerAtlas ID | HS146-06596 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr17:57928590-57930360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr17:57929988-57930003 | AGTTAATCTTTAATT | - | 6.69 | IRF1 | MA0050.2 | chr17:57928724-57928745 | AAAAAAAAAAAGAAAGAAAAT | - | 6.41 |
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| Number of super-enhancer constituents: 38 | ID | Coordinate | Tissue/cell |
SE_00167 | chr17:57928463-57931953 | Adipose_Nuclei | SE_02295 | chr17:57928689-57931238 | Astrocytes | SE_18274 | chr17:57930051-57931553 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23233 | chr17:57929107-57929676 | Colon_Crypt_1 | SE_24435 | chr17:57929181-57929542 | Colon_Crypt_2 | SE_25771 | chr17:57928325-57931576 | Duodenum_Smooth_Muscle | SE_27082 | chr17:57928496-57929857 | Esophagus | SE_27082 | chr17:57929879-57931697 | Esophagus | SE_27746 | chr17:57928616-57929834 | Fetal_Intestine | SE_28673 | chr17:57928917-57930216 | Fetal_Intestine_Large | SE_30688 | chr17:57928727-57929905 | Fetal_Muscle | SE_31691 | chr17:57928467-57929850 | Gastric | SE_31691 | chr17:57929889-57934183 | Gastric | SE_33772 | chr17:57928460-57936020 | HCC1954 | SE_34288 | chr17:57929052-57929774 | HCT-116 | SE_34288 | chr17:57929982-57931581 | HCT-116 | SE_34651 | chr17:57928545-57935173 | HeLa | SE_35896 | chr17:57928743-57929984 | HMEC | SE_35896 | chr17:57930167-57931624 | HMEC | SE_38158 | chr17:57929914-57934177 | HUVEC | SE_38933 | chr17:57928500-57931221 | IMR90 | SE_43382 | chr17:57928476-57938699 | MCF-7 | SE_44187 | chr17:57928558-57931254 | NHDF-Ad | SE_44824 | chr17:57928546-57931037 | NHLF | SE_45686 | chr17:57928409-57931778 | Osteoblasts | SE_47118 | chr17:57902074-57938709 | Panc1 | SE_47932 | chr17:57929206-57929630 | Pancreas | SE_50387 | chr17:57928477-57931778 | Sigmoid_Colon | SE_51624 | chr17:57928515-57931338 | Skeletal_Muscle | SE_52483 | chr17:57928510-57929816 | Small_Intestine | SE_52483 | chr17:57929846-57931663 | Small_Intestine | SE_54204 | chr17:57928446-57931483 | Spleen | SE_55059 | chr17:57928710-57929776 | Stomach_Smooth_Muscle | SE_58037 | chr17:57929089-57929753 | VACO_9m | SE_59128 | chr17:57902596-57931450 | Ly3 | SE_61214 | chr17:57902066-57937473 | HBL1 | SE_62339 | chr17:57902123-57931675 | Tonsil | SE_64271 | chr17:57930159-57931614 | NHEK |
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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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Enhancer Sequence | TCTACTGTAG GTCCAGCTAC TTGGGGGGTT GAGATGGGAG GATCATTTGA ACCCCGGGAG 60 GCAGAGGTTG CAGTGAGCCG AGATTGCGCC ACTGCACTCC AGCCTGGGCA ACAGAGAGAG 120 ACGCCATCTA AAAAAAAAAA AAAAAGAAAG AAAATGGCGA GGAAGGACCC AAAGAACCCC 180 TGAAAAGACA GCAATGCCCA TCCCCAAGCC AGGAATATAA AGGAGGCAAG TCTGAGGAAG 240 ACAGACTATT CTGTTTTGAA TATGTGGAGG GGCGATAATG ACCAATAGGA TGGTGGGGCC 300 TGTAATATTC TCTATCTTAG GCTTCCTAAC TCCTAAACTC CTAGTGAATA TGCCGTTCTT 360 TACACCACAC TGTAACTTCT GTCAGTGAAT AAGCTGGACT TCTTCAGAGA ATTCTCCAGG 420 GTAACAGGTC CTTAAGCCGT GTTATGTGGT GGTGCTGTTA AAGAGATGGC ACTGTGACTG 480 GACCTTAAGG CCACAGTAAA CTTTTAAAAT TCCTCTCCCC AGTATCCCGC TGGCTTAACC 540 AACGGCCCCT CCCTTTGAGA ACTGAGAGGA TGGTAGTTCC TGGAGAGATC ATCTGTCTTT 600 ATAAGGAGAA AAGTTTGGCA ATGTGATTTC CTGTATGTTT CTACCGGAGT CCAAGATTCC 660 AGCAGTGCTA GCCTAGACAG CAGCGGCTGC ATCCTAGAAC CCAGAGGTCA GGAGTGCTCC 720 CAAGTCAGTG TGAGGGCATC TTCCCAACTG CCTTTGCCAA GCCAAAAGGC AGAATCACGA 780 CTTTGTTACA CCTTCTGGAG CATGTGGTCG AGGCGGCTTT CCATGTGGCT GCTTTGGTGC 840 TGAGCCTGTT TACATGTTTC AGTAAATGAG TTATTGCTTA TTGAAGTTGG CTGGCTAGGA 900 GCTCGGAATA AACAACATAT AACCACAATG ACACCACTCT CCAGAAGTAC CAGAGTTCAG 960 AGGGAAAGAT CTGCTTGTAT GTTCCACTCC CACGTGGATG CGTAGTTCTC AAAGCCTGGG 1020 AGGACTGGGG TGTCACTGTT CCCGGCTTTC TGATGGAATC AGACATAATG AGATGTCTTC 1080 CTGGTAGAAA GTGTATATGA AAGTACTTTG CACAATCTCA GAAGGAAAAG GGAGGGCACT 1140 GCTTTTAGAA AAATGTATGA GATCAAAGAA GTTTTCAGAT GTTCTGCATT TTCTTCTTCA 1200 ATTATAAAGA ATTCATCTGA GCATAAAAGA CTCCCTGGTC TCTGTAAGAA GTAAAAACTT 1260 CTTTCATACA CAAAAGTTTT CCTACTTTAT ATACTTCTTT TTAGACTGTT TCATTTATTT 1320 TTTGTGGTAT ATTTATTAGT CTTCCCTGAA GTAGGCAGTG TTCATTAGAA GAACATGTTG 1380 AGACAATTAA GACCCCAAAG TTAATCTTTA ATTTCTCCCT TCTTCCTGTG CCACCTGGAT 1440 GACCTTGGAG TGTCCAGGAG TTCCTACACC CCATCTATGT GACAATTTAC AGAATAATTT 1500 TTTTTTTAAG ACAGAGTCTC ACTCTGTTGC CCAGGCTGGA GTTCACTGGC ACGATCTTGG 1560 CTCACTGCAA CCTCTGCCTA CCCCAGGCTC AAGCAATTCT CATGCCTCCA CCTCCAGAGT 1620 AGCTGGGATT ACAGATGCAT TACACTTGGC TAATTTTTGT ATTTTTAGTA GAGACAGCGT 1680 TTCGCTATAT TGGCCAGGCT GGTCTCAAAC TCCTGACCTC AAGTTATCTG CCAACCTCAG 1740 ACTCCCGAAG TGCTGGGACT ACAGGCGCAT 1770
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