| Tag | Content |
|---|
EnhancerAtlas ID | HS129-19448 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:43411310-43414190 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOS | MA0476.1 | chr2:43412524-43412535 | AATGAGTCAGA | - | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr2:43412761-43412776 | GAGGTCAGGAGTTCA | + | 6.22 | | Stat4 | MA0518.1 | chr2:43412483-43412497 | CTTCCAGGAAAACA | + | 6.01 | | ZNF263 | MA0528.1 | chr2:43412626-43412647 | GGGGGAGGAGGAGGGAAATAG | + | 6.25 | | ZNF263 | MA0528.1 | chr2:43412629-43412650 | GGAGGAGGAGGGAAATAGGGA | + | 7.67 |
|
| | Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
| SE_11879 | chr2:43411383-43412452 | CD3 | | SE_14384 | chr2:43411043-43412748 | CD4_Memory_Primary_7pool | | SE_14384 | chr2:43413219-43414592 | CD4_Memory_Primary_7pool | | SE_18565 | chr2:43411025-43413744 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19552 | chr2:43410892-43412743 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20901 | chr2:43411265-43412690 | CD8_Memory_7pool | | SE_23059 | chr2:43410730-43412603 | Colon_Crypt_1 | | SE_23059 | chr2:43412948-43413413 | Colon_Crypt_1 | | SE_23059 | chr2:43413499-43415097 | Colon_Crypt_1 | | SE_23724 | chr2:43413577-43414998 | Colon_Crypt_2 | | SE_24685 | chr2:43411668-43412670 | Colon_Crypt_3 | | SE_24685 | chr2:43412860-43413339 | Colon_Crypt_3 | | SE_24685 | chr2:43413459-43415042 | Colon_Crypt_3 | | SE_26374 | chr2:43411578-43412541 | Duodenum_Smooth_Muscle | | SE_26557 | chr2:43410683-43413501 | Esophagus | | SE_26557 | chr2:43413594-43414157 | Esophagus | | SE_27617 | chr2:43410563-43412793 | Fetal_Intestine | | SE_27617 | chr2:43413294-43415056 | Fetal_Intestine | | SE_28536 | chr2:43410698-43412841 | Fetal_Intestine_Large | | SE_28536 | chr2:43413385-43415120 | Fetal_Intestine_Large | | SE_31392 | chr2:43412057-43412502 | Gastric | | SE_34919 | chr2:43410735-43413487 | HeLa | | SE_40066 | chr2:43410642-43412853 | K562 | | SE_40066 | chr2:43412966-43414524 | K562 | | SE_49954 | chr2:43413006-43414618 | RPMI-8402 | | SE_50052 | chr2:43410675-43412799 | Sigmoid_Colon | | SE_50052 | chr2:43413429-43415196 | Sigmoid_Colon | | SE_52337 | chr2:43410711-43412808 | Small_Intestine | | SE_52337 | chr2:43412932-43414927 | Small_Intestine | | SE_53288 | chr2:43413619-43414846 | Spleen | | SE_58412 | chr2:43352450-43425007 | Ly1 | | SE_61450 | chr2:43354337-43468354 | Toledo | | SE_62203 | chr2:43354169-43468733 | Tonsil | | SE_68698 | chr2:43413313-43415346 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I043183 | chr2 | 43410757 | 43414993 |
|
Enhancer Sequence | TATCTCTAGT CCATGGTGTC TTCCCCCACC GTCCCCCCAC CCCAGTTCCC CGGCGCCCAG 60
GCAGCACCTG TAGATGAACC TCCCCTTGGC CCTACTTTGA AGGGGGCCCC TTCTCAGAGC 120
CTTTAATGGC CAGACCCCAG GATTGAGTTT TCTTGACCTG ACCTCTCCAA AGTTTCTCTC 180
TCCTTCCATC ACTGCTGGTC TCATATCAGT CCAGCTCACC CCCGCCTTCC TCCAGGAAAG 240
GACTCCTGAC CTCATTAGGC TCGCGCCCCC TCCCGCTGAC CTCCGAATGG GCTGCTACAA 300
GTTCATGGTT CACCTACAGG GAGTGGCTGC GCACACCAGT CACTGAGGTG AGTAAGTGCT 360
TCATCTCTCT CAATCCCGGA ACAGCAGACA CCACCGTCCC TAGGTGACAG AGAAGAAACA 420
GAGGTTCAGA GAGGCTTAGT AACATGCCAT GACTCACACC AGTGGTTAGT TAAAAAACCA 480
GGACTTGAAT CCAAGGCTGA CTTGATGACC GATCTGAAAA ACTTCGCTTT GTTTCATGGG 540
TCAGCAAACT ATGGTTTGAG CTCCCAAGTA GCTGAGGCTA CAGTTGACCT GTGGGCCCGG 600
TTTTACCCAC TGTCTGCTTT TGTGCAGCCT GAGAGCTAGA ATGATTTTTT ACGTGGTTGC 660
AGGGAGAAAA TCAAAAGCAG CATAACACTC TGGCACATGT GAAAATCATA TGAAATTAAA 720
ATGTCAGTGC CCGTTAAAAA ATGTTATTGA AGCACAGTTG TGCCCAGTCA GGTATGGCCA 780
AGTTGGGTAG TTGTGACAGA GACAAAAGAC TCCAAAGCCT TATTCTTTTT ACATCTGGCC 840
CTTTACAGAA AGCATTTGCT GGGCCCTGCG CTAAAGGGTT CTCCCACAGC CCCAGGGGCC 900
CTAAACACAC TGCCTGAATC TAGGGGTTGC TGGAAGACCC TGGAGGAAAA GTAAGGTGGA 960
TTTCAGCCCT TTGTACACCC AGGTACTCAA GATTTGCTAA AGGCTCAAGA CCTGAAAACA 1020
TCCAGAAAAT GCCTCTAAAC CAACCCCTAC TGGTGTTCCC CGCTGAGCCA GACTATCTGT 1080
CCGAGGGTCT GCGGTGGGAC ACCTTGGTCC CTACAGGATC TGACTCATCT GGTGGAGTGC 1140
TCTTCCGGTC TTGTTTAGTT TTCAAAGAAA CAACTTCCAG GAAAACAGCA GAAGGAAGAA 1200
GGCTTCATGG GAAGAATGAG TCAGAGAGTT GTTATGGGGA CTGCATGGGA CCCAGAAAGA 1260
AAATACTAAG CCTGAAAGGA TAGCAAGTGA CAGGTGCTGA TGACCTGCAA CTCTTAGGGG 1320
GAGGAGGAGG GAAATAGGGA ATTCTGGAAA CCTGTGTGGG ACTTTTGCAT AAATTAGAAA 1380
AAGGTGGCCG GGCGTGGTGA CTCACGCCTA TAATTCCAGC ACTTTGGGAG GCTGAGGCAG 1440
GTGGATCACC TGAGGTCAGG AGTTCAAGAC CAGCCTGACC AACATGGTGA AACTCCGTCT 1500
CTACTAAAAA TATAAAAAAT TAGCCGGGCG TGGGGGCGGG TGCCTGTAAT TCCAGTTACT 1560
CGGGAGGCTG AGGCAGGGGA ATCGCTTGAA CACAGGAGGC AGAGGTTGCA ATGAGCCAAG 1620
ATTGCGCCAT TGCACTCCAG CCTGGGCGAC AGAGCAAGAC TACATCTCGA AAAAAAAAAA 1680
AGAAGGAAAG AAAAAGGCTC CCCTTCCTCC TGCCCAACAA GGACGCCCTT GGTGAGTGGG 1740
GAGGGAGCTG TAGTTCAGCC CCGCCTTGCG CCCACCCCCA GGCCAGACAC GCTTATGTAG 1800
TGCTCCCATT TCACAGCTGT CTGTGGCAGC CTGACTTGAC CTGACAGTAG GCAGGTCCTG 1860
AACCAGCTTG GGTTTCCTGA GTTTCCCTCT AACTCTGCTC CTCACTCAAG CCAGTCCACC 1920
AGCCTTCCTG GGTTTGTTTC TTCTTCTGTA TAATGGGAAT GTCTGTCCTG TCTCCCTCCG 1980
GCAGTTCTGG GTATGCAATG ATGAAGCAGA TGTGGACACC AGGGTGGAGG GTTTTGATGT 2040
CAACCAAAGG ACCAAATGGA AGCCTTCCAT TTGGGGTCCT CCAGAAGCTG CTATTTACAG 2100
AAAAGGCTTT GTTGTCATTT TTAAAAACAG ATATGGTGAA GAAAATTTGG AAAACAGAGG 2160
GGTGTAGTGC CCACAGTCTA CCATGGCTAA CATCATTCCT ACACTCTATC TTGCTTTGGG 2220
GGCCAGGGAG GGAAGACACT TGAGCATTAC TTCTCAAATG TCTCAACTTT CCCGGAGGAA 2280
ATTGTTAAAA AGCAGGTTCT GGTTCAGAAG GCCTGGAGTG GGGCCCAAGA GTCCTCGCTT 2340
CTAACAGAGT CCCAGGTGAC GCCCATCTGA CACTCGGAGT CTCATGGGAC CGAGAAGACC 2400
TTAGCGCAGG TTGAAGAGGT GAGGCCAAGG TGTCCTTGCC CTGAGGGGTA GTGGGAGCCC 2460
TGGAAGCTCC TAGCCTGTGG CAGGCCTGCC TCTTGAAGTA AGGCACAGGG GCAGCCTCCC 2520
AGGACCCCGG GGATCAGCCA ACAGGCTCCA CACTGGAAAC TGTGGGAGTG AAGACCTCAA 2580
GGGCTCAAGC CCTTGGGCGG GGGTGGGAGG AGGTCTCGAG CTGGGGAGGC TGGGAAGGGC 2640
TGGGTTTCCC CAGATCAAAG CAGCTTCCCC AGCCTTTGAT TCCCCAACAA GCAGCCTCTT 2700
TGGACTCGGA CTGGAGTTTG GGGCCCGCTG GTCTTAGGGC CTGGGGAAAG TGGTAAGAGG 2760
CTCTGGCCTG CTCTCTTTTT GCATAACAGC TTGGCTGCCT AACAAAAGGG CGGTCCTTAA 2820
AAGGCCTTAT GGGGCTGTTA AAAGCTTCCG GCGATGGTTT AATTGGGGGC GATTAAAGTG 2880
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