| Tag | Content |
|---|
EnhancerAtlas ID | HS060-16436 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr19:957600-960090 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr19:957894-957909 | GAGGTCAGGAGTTCA | + | 6.22 | | Zfx | MA0146.2 | chr19:958653-958667 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27633 | chr19:948842-958164 | Fetal_Intestine | | SE_27633 | chr19:958212-964328 | Fetal_Intestine | | SE_28572 | chr19:950271-958034 | Fetal_Intestine_Large | | SE_28572 | chr19:958119-964436 | Fetal_Intestine_Large | | SE_57993 | chr19:952760-957893 | VACO_9m |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I000942 | chr19 | 942421 | 964263 |
|
Enhancer Sequence | GAAGGCAACA CGTGAGGATC GAGGGAGCCC AGGAGGTCGA GACCAGCCAG GGCAACATAG 60
AAAGACCCAT CTCTACAAAA GAAAATGTAA AAACTTAGCC GGGTGTGATG GCGAGTGCCT 120
GTGGTCCCAG CCACTTGGGC AGCTGAGGCA GGAGAATCCC TTGAGCCCAG GAGGTTGAGG 180
CTGCAGTGAG CTATGATTGC GCCACTGCAC TCCAGGCTGG GCAACAGAGT GAGACCCTGT 240
CTCCAAAAAC AAACAAAAAA AAGACTTTGG GAGGCTGTGG CAGGCGGATC ACTTGAGGTC 300
AGGAGTTCAA GACCAGCCTC GCCAAATAGT GAAACCCTGT CTCTACCCAA AAAATACAAA 360
AATTAGCTGG GCATAGTGGC AGGTGCCTGT AATCCCAGCT ACTCAGGAGG CTGAGGGGGG 420
AGAATTGCTT GAGCCCCGGA GACAGAGGTT GCAGCGAGCT GAGATTGCGC CATTGCACTC 480
CAGCCTGGGC GACAGAGCGA GACTCCATCT AAAAATAATA ATAATAAAAA TTAAAATTAA 540
AAAAAAAAAT AGGCTGGGCG CAGTGGCTCA TGCCCATAAT CCCAGCACTT TAGGAGACTG 600
AGGCAGTCGG ATCACGAGGT CAGGAGACCA TCCTGGCCAA ATGGTGAAAC TCCGTCTCTA 660
CTAAAAATAC AAAAAAATTA GCCGGGCGTG GTGGCGGGCG CCTGTAGTCC CAGCTACTCC 720
AAGAGGCTGA GGCAGGAGAA TGGCGTGAAC CCGGGAGGTG GAGCTTGCAG TGGGCCAAGA 780
TCGCGCCACT GCACTCCAGC CTGGGCGACA GAGCGAGACT CCATCTCAAA AAAAAAAAAA 840
AAAAAGAAGA AAGAAAAAGA AAAGAAGAGG ACAGGTTCAA GCACTGGATT CCCAGTACCT 900
GTGACAGGAC CTCATTTGGA AACGGGGGAA CTTACTGACA TACAATCACG TGTTGACACT 960
TTGGTCAACC TCAGACCGCA GATGGGACGG TGGTCCCACA GGATTAGAAT TCCATATTTC 1020
TAGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG AGGCGGGCGG ATCACGAGGT 1080
CAGGAGATCG AGACCATCCT GGCTAACACG GTGAAGCCCC GTCTCTACTA AAAATACAAA 1140
AAATTATCCG GGCGTGGTGG CGGGCGCCTG TAGTCCCAGC TACTCGGGAG GCTGAGGCAG 1200
GAGAATGGAG TGAACCCGGG AGGCGGAGGT TGCGGTGAGC CGAGATTGCA CCCCTGCACT 1260
CCAGCCTGGG GACAGCGAGA CTCCGTCTCA AAAAAAAAAA AATTCCATAT TTCTTGTGCA 1320
CCTTTTCTGT GTTCAGCTGT GTTAGACGCA CAGACACTCA TGCTCACGTT GCCACTGCCT 1380
ACGGGACCCA GGACAGCCAC AGATTTGTAG CCCAGGAGCG CTGGCTGGGC TGTGCCTGTG 1440
CCTGGGTGTG TGGGAGGCTC CACCCGTGAG GTGTGTGTGA CTCACTGTTT GATGTTCACA 1500
CTGACGAAAT CACCAACAGA CATTTATCAG GACGCATCCT GCACGAAGAC AGAGGCAGAG 1560
GCTGGAGCGA CGCGGCCACA AGCCCAGGAA CCTGGAGCCC CCAGAAGCCG TGAGAGGCAG 1620
GAAGGTTCCT CCCTTGGAGA CTTCGGAGGG AACGCAACCC TGCAGACATC TTTTGTTTTG 1680
TTTTGTTTTT AGAGACAGGG TTGCGTTCTG TCGCCCAGGC TGGAGTGCAG TGGTGCGGTC 1740
TCGGCTCACT TCAGCCTCCA CTGCCCAGGC TCAAGCAATC CTCCCACCTC AGCCTCCCGA 1800
GTAGCCGGGA CTGTAGGCAT GAGCCACCCC ACCTGGGTAA CTTTTTGTTA TCATAATGTA 1860
GAGATGGGGT CTCACTATGT TGCCCAGGCT GGTCTTGAAT TCCCGGGCTC AAGCGATTCA 1920
CCCGCCTCCC AAGGTGCTGG GATTACAGGT GTGAGCCGCC ACCCTGAAGA GAAGTTGGTT 1980
TTGGACTTCT GGGCTCCGGG ACCGCGGGAG AATAGATTTC TGTTGCTTTA AGCTGCAACG 2040
TGTGGCTGTA AGGGAGTTAA GGATCGATTT GAGATGAGGT GGCCCTAAAA CCAGCAGGCT 2100
GGTGTCCTGA GAAGAGGAGA GAGAGACGGG GAGACGGTCT TGTGGAGACG GAGGCAGAGA 2160
CTGGAGCGCT GCGGCCACAA GCCAGGACGC ACCTTGATCT GGGGTTCCCG GGCCCCTGGA 2220
CCGGGAGAGG ACACTGTCTT GTCCCAGGCC ACCTGGTTTC TGGTGCCTCC TTGCAGACCC 2280
TCTGGGAAGC TCGTTCACCG GCATTTCTGT CTTGCAGCCT TGTGGTTCTT CACCTGCCCA 2340
GCGGGGTCTT CGGCTCTGGC AGCGGCTTGA GGGTCCTAGG GGTGGTGACC CCTGCTCCTG 2400
TCCTCCTGAC CTGGCCTCCA GTGCAGGAGG GACATGGTTC CCACACCTGA GCTCTGGCAC 2460
CAACTAACCC ATCCCCTCTC CACCCTCACA 2490
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