Tag | Content |
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EnhancerAtlas ID | HS074-02425 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr11:34655150-34656210 |
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 | TGATAGGTTG TCCACAGAGG CCCACAGAAA ACAAGCAAAA CCAGGAGGAT GTAAATGTTT 60 GGAAGAAGAG GAGAGTCAAA GTTTCTTTTG AGGCCTCAAA AGCCTCTGTG ATGTTTTACA 120 ATCTGAAGCT TGCCCTATTC TTAATCATAT CTGATGGGTT TGATAAAGGC CCTGGGGGTC 180 ATCTTAGGCA AGCTTGTCTT TTGATCAACT TGAGTGCCTG CCACTGTCAG TATGTGCTGC 240 CTAGCCTGGG TCTGACACCA AGACTGATAA AGATCAGCAT ACTATGTATA TTTCCAAATG 300 GCTTACAGTC AATAAAGTGT ACCTATAATG GATCCAGACT TGGCCTCCCA GTGCTGCATT 360 ATTGGTCATG AAAACCCTTG AAACCCCAGC AATAATACCT CAGATGTTGC CCCTGGGAAC 420 GTGAAAAATG TCTGTTTCAA AACACATTAT AAGGCTATGA AATTATCTGT GATGTAATCC 480 CAAGAGAATC AAATACATTC CCCAAGCTTG ATTCACAATT CAATTCATTT GTAAAAACAC 540 AAATGATTGT ATGTATTATA TTCAGTTGCC TTTCACATGT ACATGGATTT TTTTTTCTCT 600 TATTTGGGAG TAGTCCTTTG AAACGACAGT CATATTGAAA CAGGAAGTCA GTAAGCTGTT 660 GCAACATCCT TAGGGCAAAT GCTGTGAATT CACCTGCTGG TAACTTTGAT TAAGGACTGA 720 GAATGGTGTG GGTATCGCTG TCATCACAAA AGTAATTATT TAAAAGGACT AATTGCTCCT 780 TTGGCTTCAG AGGTAAAAAT GCCCACATGG CAGCCAGTTC TGTGGCAGTT TGGGGATAAT 840 GTGGTTGGAT GAATAAGGGA GCTAGGAAGA AGGCTGATGG TGGCCTTGAC TCTCAATCCC 900 CTGGGGCTGG GGACAGGGAA TGCAGGTGCA AGCCCTGGTT AAGATCTGCT CCGTGGCCCT 960 GGTGGTTCCC AGTGTACCTT CACCCTTGCA GCAGGAGCAA ACCATGCTGT CTGGCCTGAG 1020 GTCTGATTCA GGTAAAGCAT AAACAATTAT GGACCAGTCG 1060
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