Tag | Content |
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EnhancerAtlas ID | HS060-05452 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:34655320-34656210 |
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) |
Nkx2-5(var.2) | MA0503.1 | chr11:34655358-34655369 | CTTGAGTGCCT | - | 6.14 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_23244 | chr11:34654801-34655718 | Colon_Crypt_1 | SE_23244 | chr11:34655758-34658352 | Colon_Crypt_1 | SE_26655 | chr11:34651923-34657750 | Esophagus | SE_31738 | chr11:34651980-34656657 | Gastric | SE_33847 | chr11:34652014-34656871 | HCC1954 | SE_34914 | chr11:34652697-34657449 | HeLa | SE_41618 | chr11:34655304-34656519 | LNCaP | SE_50680 | chr11:34652022-34658416 | Sigmoid_Colon | SE_52951 | chr11:34654912-34658271 | Small_Intestine | SE_57552 | chr11:34655816-34656304 | VACO_503 | SE_58084 | chr11:34655883-34656204 | VACO_9m | SE_64547 | chr11:34654667-34656518 | NHEK |
|
| Number: 1 | ID | Chromosome | Start | End |
GH11I034630 | chr11 | 34652083 | 34657669 |
|
Enhancer Sequence | CCTGGGGGTC ATCTTAGGCA AGCTTGTCTT TTGATCAACT TGAGTGCCTG CCACTGTCAG 60 TATGTGCTGC CTAGCCTGGG TCTGACACCA AGACTGATAA AGATCAGCAT ACTATGTATA 120 TTTCCAAATG GCTTACAGTC AATAAAGTGT ACCTATAATG GATCCAGACT TGGCCTCCCA 180 GTGCTGCATT ATTGGTCATG AAAACCCTTG AAACCCCAGC AATAATACCT CAGATGTTGC 240 CCCTGGGAAC GTGAAAAATG TCTGTTTCAA AACACATTAT AAGGCTATGA AATTATCTGT 300 GATGTAATCC CAAGAGAATC AAATACATTC CCCAAGCTTG ATTCACAATT CAATTCATTT 360 GTAAAAACAC AAATGATTGT ATGTATTATA TTCAGTTGCC TTTCACATGT ACATGGATTT 420 TTTTTTCTCT TATTTGGGAG TAGTCCTTTG AAACGACAGT CATATTGAAA CAGGAAGTCA 480 GTAAGCTGTT GCAACATCCT TAGGGCAAAT GCTGTGAATT CACCTGCTGG TAACTTTGAT 540 TAAGGACTGA GAATGGTGTG GGTATCGCTG TCATCACAAA AGTAATTATT TAAAAGGACT 600 AATTGCTCCT TTGGCTTCAG AGGTAAAAAT GCCCACATGG CAGCCAGTTC TGTGGCAGTT 660 TGGGGATAAT GTGGTTGGAT GAATAAGGGA GCTAGGAAGA AGGCTGATGG TGGCCTTGAC 720 TCTCAATCCC CTGGGGCTGG GGACAGGGAA TGCAGGTGCA AGCCCTGGTT AAGATCTGCT 780 CCGTGGCCCT GGTGGTTCCC AGTGTACCTT CACCCTTGCA GCAGGAGCAA ACCATGCTGT 840 CTGGCCTGAG GTCTGATTCA GGTAAAGCAT AAACAATTAT GGACCAGTCG 890
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