Tag | Content |
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EnhancerAtlas ID | HS095-05971 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:95991140-95992930 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr11:95991149-95991160 | TTTTATGGCCT | - | 6.02 | Foxd3 | MA0041.1 | chr11:95991514-95991526 | AAATGTTTGTTT | + | 6.27 | Gfi1b | MA0483.1 | chr11:95991686-95991697 | AGCTGTGATTT | - | 6.14 | IRF1 | MA0050.2 | chr11:95991347-95991368 | TTACTGAAAGTGAAACTTATA | - | 6.64 | IRF1 | MA0050.2 | chr11:95991563-95991584 | AGAATGAAACTGAAAGAGGCA | - | 6.76 | IRF2 | MA0051.1 | chr11:95991351-95991369 | TGAAAGTGAAACTTATAA | + | 6.4 | IRF8 | MA0652.1 | chr11:95991350-95991364 | CTGAAAGTGAAACT | + | 6.19 | Lhx3 | MA0135.1 | chr11:95991185-95991198 | AATAAATTAATTT | - | 6 | TBP | MA0108.2 | chr11:95992060-95992075 | CCCAGCCTTTTATAC | - | 6.22 | ZBTB18 | MA0698.1 | chr11:95992404-95992417 | TTTCCAGATGTTT | + | 6.28 |
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| Number of super-enhancer constituents: 22 | ID | Coordinate | Tissue/cell |
SE_00421 | chr11:95990695-95994185 | Adipose_Nuclei | SE_09528 | chr11:95988993-95993093 | CD14 | SE_10685 | chr11:95986205-95993908 | CD19_Primary | SE_11167 | chr11:95985208-95994550 | CD20 | SE_12380 | chr11:95989202-95994108 | CD3 | SE_15173 | chr11:95986487-95994286 | CD4_Memory_Primary_7pool | SE_16197 | chr11:95990631-95994008 | CD4_Naive_Primary_7pool | SE_17498 | chr11:95985112-95995021 | CD4p_CD25-_CD45RAp_Naive | SE_18301 | chr11:95989089-95994399 | CD4p_CD25-_Il17-_PMAstim_Th | SE_30644 | chr11:95990730-95992362 | Fetal_Muscle | SE_31211 | chr11:95989224-95993674 | Fetal_Thymus | SE_36675 | chr11:95990838-95992393 | HMEC | SE_36675 | chr11:95992462-95993458 | HMEC | SE_44431 | chr11:95990759-95993077 | NHDF-Ad | SE_45599 | chr11:95989581-95994498 | Osteoblasts | SE_50559 | chr11:95991362-95993946 | Sigmoid_Colon | SE_53120 | chr11:95991353-95993089 | Small_Intestine | SE_54051 | chr11:95991340-95993046 | Spleen | SE_58447 | chr11:95917840-96001635 | Ly1 | SE_61108 | chr11:95917662-96027831 | HBL1 | SE_61760 | chr11:95940172-96001818 | Toledo | SE_62369 | chr11:95920962-96006907 | Tonsil |
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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 |
GH11I096253 | chr11 | 95986252 | 95993991 |
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Enhancer Sequence | TGATCCTAAT TTTATGGCCT GTTCAAATAT TACAACTTCT TTTTAAATAA ATTAATTTGG 60 AACTAAATGC CTTTAATTTT TACCGTGATA GGTTTGTGGC TCTTGACATC TTTTGGTCCT 120 ATTCATCAAA ATCATTTGCT AAGTCCAAGG TATAGCAGAG TGGCTTTAAC AACAACCATG 180 GAGGATGAAT AAAATACATT TTCATATTTA CTGAAAGTGA AACTTATAAG CATATATCAT 240 CTTCTGCCTA CCTTGTAAAT ATCCCATGTT TTCATTTACA TATTGTACCA ATTAATATAT 300 CTTGGTACTA ATCAGAGTGG AATCCACTCC TGACATGGGA GAAAACTACG ACAAAAAACA 360 TTAGCAGCAA GAAAAAATGT TTGTTTCAAG TATGTGGATT ATATTTTCTA GTGCCTTAAA 420 AAAAGAATGA AACTGAAAGA GGCAGCTTGA AGAAGCTTAC ATGTGTTTAA AACCCACATC 480 CTGTTGTTAT CCACTGCCCT GGCACAGAGG AGCTGGGAGG TGAACGTCCT CATTAGGGTC 540 CCTATTAGCT GTGATTTGCA ATGGGCTTCT CCAAAGAAGA AAATCACATT CACCCACTGG 600 ACAATGGCCC AGGTATCACC ATTGATGGGA ATCATATATG GAGTAAACAT CAAAGCCCAA 660 GAATACAGTG GTCTAAGCCA GTGTGCTTAG AAGTTGCCAG ATCCTCCATG CTTCATTCCA 720 GCCACTATCA GCAGATTCTA AATCACCTAT GAGCAGAGAG GCCCATCTGC CTAGGGCATA 780 AACGAAATTA TAACAACAGT GAGAGAGCCA ATGGGAGTCA GCCAGTAAGA CTATGAGCAG 840 CATGATGTAC TCAGACTTTT GTTCCTTTTT ATTTATTTGG TTAAAATACA TGTGTTTTTG 900 CTTCAGGCAG ATGTTGGTAT CCCAGCCTTT TATACAGGAA GCTGTAGAAG GGAGAGGACT 960 TTCTGGGTGG GAGCAACTTA TTGTGGAGGC CAAATGGCAT TTTTTGTAGG CCCTGAGATT 1020 TTTTACGAAA ACACTAACTC TGTTCAGAAC TCTTTCAAAG GGTGAAGACA AACTTAACAA 1080 CCTTATACTA TAATACAAAT AATTACAGAG TGTTGCTTTA AACTTGTATC TTGAAGTTCC 1140 TTCTTTAGGT AACTCTGCTT AACAACCACA GACTCTTCTT CCTAATGGCT TATCTGCATG 1200 TCTTTTCAAT TTTCTAAGTG AAGGCCAGCC CCCTTCAAGA TGTTCTACCA ACTCAGTCCT 1260 ATTCTTTCCA GATGTTTTTT TTCTTTTTCT TCTTCTGAAA AGCATGTGTT GATAGACTAT 1320 GGGGAACAGA CCAAGATTTA TTTTTTAGCC AGCATTTTCC CCTTGCAACC GTAAGTCATT 1380 CTTCCTCAGA AGGCAAGGTG GGGCAAGTGA TTCTAATGTG CTTCGCTCCA ATGCTTCCAT 1440 CTCAATAACC CTTTAAAGTG AAAACTGTGG AGAGTGAAGT GAAAAACTTG TCTCCATCTG 1500 GAAGCATTTA TACAGAGAGG TGTCTTTAGC TTAGTTGTTT GTCTAGAATT TCCATTTATG 1560 AACCGACTTG CCTTTCTCCT GTGGGTATGC TGGAGAAAAC TCTTTGCAAA ATCCATTGTA 1620 TGCAATAATC CAGTGGCTCC TTCAAACTCA ATCAGGCTGG AAAGGCTAAA TATGACTCAT 1680 AGGATTCCTC CAACAAACAC AAAGTAAGTC AGAAGTCAAG GAGAGAGTCA TCTCGATGTG 1740 GACCAGCTTA CCTAGCAAGG CAGGGAATTG TCATAAAACC AGTTTCCTGC 1790
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