Tag | Content |
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EnhancerAtlas ID | HS060-25191 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr3:141055390-141056700 |
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) |
INSM1 | MA0155.1 | chr3:141055687-141055699 | TGCCCCCAGGCA | - | 6.04 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_27685 | chr3:141053865-141056982 | Fetal_Intestine | SE_28664 | chr3:141053882-141057027 | Fetal_Intestine_Large | SE_45548 | chr3:141049278-141057206 | Osteoblasts | SE_55659 | chr3:141048658-141057238 | u87 | SE_67471 | chr3:141048658-141057238 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I141335 | chr3 | 141054171 | 141057149 |
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Enhancer Sequence | GTGTTGGCCA GGGTGGTCTT GAACTCCTGG CCTCAAGCAA TCCTTCCACC TCAGCCTCCC 60 AAAGTGCTGG GATTACAGGT GTGAGCTACC ACACCTGGCA GTAATAGATG AATTTACTTG 120 TACAACAAAC ACAAATTTTT GTGTTGTGCG GTTTCTCACT AGGGCCACGG TCGGCCTCTG 180 GGCAGAGATA CTATTATGTG GTGTGGGATT TTCCCACATG GTAGGACATT TAGCATCCCC 240 CGTCCCTGGG GAACTAAATG CCAGTAGCCC CCAGGAGAAT TTGTGACATC CAGAAAATGC 300 CCCCAGGCAT TTCCAAACAC CTTCTGATGG GTGAGACTGC CCATTTGAGA ATCACTAGGC 360 AGGGAAAAGT AAATTCCTTC ATTTTACTTC AAATGGGGTG TGTTAGCATC ATCTTGCTTG 420 AGCAGCTTTA AAAAAATAGT TTCTAATTAC GTACATAACA CATTCTCTTT GCAAACAAAT 480 CCTATAGATA AAGCTGAAGT CTCCTTTGAC GCCCACTTCC AGTTCTAGTC ACTCCCCGCT 540 TCTCTGAGGA AGTGAGAGTA ACTGACATGG TTTCTACCTT CAAGACCCTT TGCTTTATGT 600 TTATATACAG ATGTAGGAAC CTGCATACAA GTATAACGGA GTGTTGTTGG TGTGTGTTTG 660 TGCTGTGTAT TTCATCTGCA ACTTGAATTT TTTACTCCAC AATACCTGTT GAAGGTCTTT 720 CCATGTCCAA ACACGTAGAA ATGCCTCATC CTACAGCCGA GTAATATGTA ATGACTGCAC 780 AGCATTTTAT CATGTTGATG GGCCTCTTAG CAAAGAGCTG CAAAGGAAAT CAATTCCCTG 840 GATGAGGCGT TGCCTGTGGT CTGGTCACAG GACCAAATTA GACAAAAGCT GAGGTCATTT 900 TGAATCATCC CCTCCAACCC TGCCGCAGTC CACAGAACAA AGCAGTGGCC TGACTTGAAT 960 TTGAACATAG TATCTCTAAG CCTGGGTATT CTGGCATTGT GTAAACACAG ATCTCTGAGC 1020 CTACTGCACT GAAATGGATT CATTTCCTTT TTTAGCTTCT GGCATGGCAT TTTTAGTTGA 1080 TAAATTGTGG TTCTAAGGAA GCAGGTTTGA TGATCCCCTT TGTCCTTCAA CCAAGTGTGT 1140 AAAGGAGGAT GTTTACTTTT ATGGGTAATT ACAGGTCTAT GAATTGAGCA CTTAATATGA 1200 GGCACCTTCA TCCCTTATCT CAAGTCCTCA CAACAGTCCT TTGCAGGAGG TATTACTAGC 1260 TCATTTTTGC AGGGAAGAAA ACTGAGACTT GCGGAGATTA CATAATTTGT 1310
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