Tag | Content |
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EnhancerAtlas ID | HS180-15058 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr14:69411900-69413650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR1 | MA0112.3 | chr14:69412827-69412844 | CAGGTCACCGTGCCCCG | - | 6.41 | ESR2 | MA0258.2 | chr14:69412828-69412843 | AGGTCACCGTGCCCC | + | 7.41 | Foxd3 | MA0041.1 | chr14:69411929-69411941 | AAACAAACAAAC | - | 6.32 | HNF4G | MA0484.1 | chr14:69412530-69412545 | AAGGTCCAAAGTCCT | + | 6.02 | Klf1 | MA0493.1 | chr14:69412404-69412415 | GGCCACACCCA | + | 6.62 | Myog | MA0500.1 | chr14:69412069-69412080 | CTGCAGCTGTT | - | 6.02 | Nkx2-5(var.2) | MA0503.1 | chr14:69412711-69412722 | AGCCACTCAAG | + | 6.62 | Tcf12 | MA0521.1 | chr14:69412069-69412080 | CTGCAGCTGTT | - | 6.62 | ZNF263 | MA0528.1 | chr14:69412437-69412458 | GAAGGAGGAACAGGCAGAGAG | + | 6.27 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_01544 | chr14:69411920-69417098 | Aorta | SE_09473 | chr14:69411857-69420150 | CD14 | SE_17458 | chr14:69410354-69416786 | CD4p_CD25-_CD45RAp_Naive | SE_22077 | chr14:69411911-69413643 | CD8_Naive_8pool | SE_24115 | chr14:69411938-69413605 | Colon_Crypt_2 | SE_25810 | chr14:69411075-69417124 | Duodenum_Smooth_Muscle | SE_26589 | chr14:69411934-69415136 | Esophagus | SE_28065 | chr14:69411629-69413701 | Fetal_Intestine | SE_28974 | chr14:69411656-69413729 | Fetal_Intestine_Large | SE_31722 | chr14:69411909-69413688 | Gastric | SE_36138 | chr14:69404230-69420474 | HMEC | SE_37016 | chr14:69402168-69421041 | HSMMtube | SE_42569 | chr14:69412546-69416585 | Lung | SE_45678 | chr14:69402257-69421189 | Osteoblasts | SE_48719 | chr14:69413196-69415134 | Right_Atrium | SE_50146 | chr14:69404175-69415137 | Sigmoid_Colon | SE_52189 | chr14:69411918-69412792 | Skeletal_Muscle_Myoblast | SE_52675 | chr14:69411335-69415129 | Small_Intestine | SE_53596 | chr14:69411943-69413699 | Spleen | SE_54485 | chr14:69401836-69420919 | Stomach_Smooth_Muscle | SE_64004 | chr14:69411904-69413077 | HSMM | SE_65495 | chr14:69411962-69413487 | Pancreatic_islets |
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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 |
GH14I068931 | chr14 | 69397719 | 69420516 |
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Enhancer Sequence | AAGAAAGAAA GAAAAGAAGA AGAAGAAGAA AACAAACAAA CAGCAAAGGC CCCAGAGAAA 60 AGAGAGTAAG GTCTGTTCAA AAAACTGAAA AAAAAAAAGT CACAGTGCAG GAGGGAAGAA 120 GAGGGTGCCA GAGACTGGAG ATCAACTAGC CACATGGGTG TTCGGGTTCC TGCAGCTGTT 180 GTTTCTCCTG AGAGCAGTGG AAGTCACCGA AGACATTTTA TTTTAGCTGA AAGAAACAAA 240 TGGGGCTGTG GCGGGCTGAG TTGGGCTGGG AGTGCCAATC AGATGCTGGT TACATAATTC 300 CACCTGCATC TTAGAAAGAG ACCTCTAAAT GCCATGGGAA GGGCAGATCA GAGATGGAAA 360 AGAGTGGCTG AAAAGAGACC AAGCACAAGA TCACGAAAAG GTCCCAGCCA GAGACAAAGG 420 GAGCCAGTCC AGGGTGGCAG TGTAGGAGAG GGAGAAGCAG GTGGATACAA GAGATACTCA 480 GGAGAGACGG GGAGGAGGGG CAGAGGCCAC ACCCAGATTT TCAGACCTGA GCCAACAGAA 540 GGAGGAACAG GCAGAGAGGC CACAGCTTTG CACCCATACT CCCTGCCTGC CCAGACACCT 600 GGGGCAGCTC GCTGTTCACA GCAGTCCCCA AAGGTCCAAA GTCCTGAGGC TGCAGATCTA 660 ATTGAAAGGT CTGAGTGGAA GAGCTTCAGA GATCAGGATG TCACTCCCAA CCCACTGCCC 720 CAAGTGTTCT ACCAGTGTCA ACCCAATCAA TCTTAACCAC CCCAGAAGGC ATCTCATTTT 780 ACAGATGAGA AAACCGAGGC CAAGAGCTCA CAGCCACTCA AGGTCACAGC GAACAGTAGA 840 TGCAGGAGCC AGAATTCCAC CCGCGGTGGC AGTCACACAC TTTCAACCAC AGGCTCAGTC 900 AGCGTGACTC TCCCCAGGGC CTGGCAGCAG GTCACCGTGC CCCGGCCACA CTCTCACAAC 960 TGTCCGTAAC AGGGCCCCTC CGCTCACAGC CCACCAGCCC ACCAGCCCAC CTCACCACCA 1020 CCAATCAAGT CACCCTCTGG GGGTGGGGCC CAGCAGAGGT TGAAATCCTC CTTAAGGGCC 1080 TCTTAAGGGT AAACTGGAAA GGATGACATA GTAAGGACCT AAAAGGGGTT TTCTCTAATG 1140 GACCAGGCCA ACTTTGAGAA GGAGGAAGCA GACAAGGCAG TGGGACCCCA GTTCCTGGCA 1200 TCATCAGCTG ACCCTGGAAA TACCTATTCC TCAACTTCCC TATCTGAACA AGGGAGCCAG 1260 CCCTGCCTGT GCTTCTAGAA AACTTCCCAG CCCAATAAAA AAGGCAGAGG AAGAGGGGAG 1320 AAGTGGCAGA AGTCCTACCC ACAGGACTTC CAGGACTCCA CCAGCAGCCC TGAGGAGGAG 1380 TCCCAGCCCC TCCCGCTGGG TCCATGCTGC CTAAGACCGC GCCTACGCTC TGACACCTGT 1440 GGATTCCCAG TGGTTCTAAG AAGCCCAAGG CCCCACATGC TCACTGGGGC CCTGGTTTTC 1500 AGAAGGCACA CCTGGGGAAG CATCCTAGTG GGGCTCAGGG CTCTGTCCCA CCATCCATCC 1560 CCCACTTAGT CTCTGCAGGT TCCCAAGGCC ATCATGGAGG CCCTCAGCCC TCACCTCCTT 1620 CCTGTCACTC CATCTCTCTC CATCCCCACC TTCACCTTTT CCATGCTTTA GTGGAATGTT 1680 TGCAGGCACA ATGGACACAC ATCACTGGGA GATCTCAGTT CTAAATCTGC TTCCACCACA 1740 AGGAGCTCAG 1750
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