| Tag | Content |
|---|
EnhancerAtlas ID | HS007-00172 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:17919400-17922200 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr1:17921150-17921162 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr1:17921150-17921162 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr1:17921149-17921164 | TTCTATTTTTAGTAG | - | 6.57 | | ZNF263 | MA0528.1 | chr1:17921489-17921510 | TCTTCAGTCCATCCCTCCTCC | - | 6.18 | | ZNF263 | MA0528.1 | chr1:17921503-17921524 | CTCCTCCCTACCTCCTCCTCT | - | 6.44 | | ZNF263 | MA0528.1 | chr1:17919474-17919495 | CTTTCCTTCTTTTCCTTCTCC | - | 6.84 | | ZNF263 | MA0528.1 | chr1:17921500-17921521 | TCCCTCCTCCCTACCTCCTCC | - | 7.15 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_01537 | chr1:17918090-17921538 | Aorta | | SE_01537 | chr1:17921744-17927542 | Aorta | | SE_23081 | chr1:17919473-17921123 | Colon_Crypt_1 | | SE_23081 | chr1:17921201-17925643 | Colon_Crypt_1 | | SE_23747 | chr1:17920285-17921075 | Colon_Crypt_2 | | SE_23747 | chr1:17921244-17921600 | Colon_Crypt_2 | | SE_23747 | chr1:17921758-17924697 | Colon_Crypt_2 | | SE_24767 | chr1:17920159-17921154 | Colon_Crypt_3 | | SE_24767 | chr1:17921216-17924712 | Colon_Crypt_3 | | SE_28131 | chr1:17921123-17925727 | Fetal_Intestine | | SE_29073 | chr1:17920969-17925491 | Fetal_Intestine_Large | | SE_40808 | chr1:17918328-17921403 | Left_Ventricle | | SE_40808 | chr1:17921758-17923372 | Left_Ventricle | | SE_49224 | chr1:17919616-17921566 | Right_Atrium | | SE_50079 | chr1:17918225-17921604 | Sigmoid_Colon | | SE_50079 | chr1:17921723-17925480 | Sigmoid_Colon | | SE_52601 | chr1:17921731-17924732 | Small_Intestine | | SE_57000 | chr1:17920348-17921020 | VACO_400 | | SE_57000 | chr1:17921204-17921634 | VACO_400 | | SE_57000 | chr1:17921741-17924705 | VACO_400 | | SE_65277 | chr1:17920806-17921493 | Pancreatic_islets | | SE_65277 | chr1:17921749-17924817 | Pancreatic_islets | | SE_68684 | chr1:17919685-17920795 | H9 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I017593 | chr1 | 17920434 | 17925458 |
|
Enhancer Sequence | TCTTTCCATT AAAAATCTTT CTTTAAAGGT CCCTTGCCAA ATCCATAAAT TGGACAAGCT 60
GGTTTTTGTG TTTTCTTTCC TTCTTTTCCT TCTCCGAGGG TAGAAACAAG GGCTCCCAGT 120
TTCCAATCAG AGCCAGGACC TTTGGATCCC AGGCCCTTTG AGGACCCCCA CAGCCTCTTC 180
ATTGAAGAAG GCACTTGCAG GGTACCTGGT TGGCACATCT CTTCATGGTA TAAATATGCC 240
TTCAAGGAAT CCTGTGACGT TCCTCCCTGC ATCCCTGCAG CGGTGGGACT CTGCCTCACT 300
CGTTTTTTAT CCCAGTGCCT GGCAGAGATG GTGCAACAAT ACTAACAGCC TACACGTGCA 360
CGGACTTTAC AGTTTACATC TCATTTTGAT TCTCACAACT GTGGGAGGCA GAATCATGGC 420
CCTTCCACCC CTTGGAGATT TCCGTGTCTT CATCCCCAGC ACCTGTGAAT CTGTGACGCT 480
GCGTGGCAAA GGGACTTGGC AGATGTGATT AAGTGAGGGG TTTTGAGATG GGGAGATGAC 540
CCTGGGTTAT CTGTGGGCCC AGTGGCACCA CAAGGGTTGT GACAAGAGGG AGACAGGAGG 600
GCCAGAGTCA GAAAGAGGTG GGAAGATGCC ACGCTCCTGG CCTTGGAAAT GGAGGACGGG 660
ATTGTGACCA AGGAATGCAG GTGGCTTCTC GAGGCTGGAA AAGGTGGGGG ATGGCTTCTC 720
CCCTGGAGCT GCCCCTGCTG AAACCTCGCT TTTAGTGAGA GCACAGCCCT GCCGAAACCT 780
CGCTTTTAGC CCTGCGAACC CCTTGATGGC CTTCTGACCT CCACACCTGT GAGAACAGAT 840
TTGTGTTGTA AGTCACTAAG TTCGTGGTCA TCTGTTACAG CAGCCATAGG AAACTAACAC 900
GACAGCCCTG GAAAGAGGAA ATTATCGTGG GCACCATTTT GCAGACCAGA CCTGGGAGAG 960
AGCGTCACTT GTCTGTGGGG CTGGGCTGGC AGGCATGGTG CTTGGGCTCA AAGCCTCAGG 1020
CCAGGGGCTC TGTTTGCCCT TTCTCTATGG CCCTCTCTGT GCATCTAGGA TGGTGCTCTG 1080
CTGACTGGCC GGTATTCCCC TGCCCTTCCC TTGCGTCTTC CTGTCCTTTC ACCCAGCACC 1140
TCTTTACTGA GTGACTGCGA TGGGGGCTGA CATGCTCTGC CAGGCCATGT TATTTTTATG 1200
TGCCTGTGTG TGTGTTTGGC TCTAGGGCCA GATCATAATG GCCTGAATGT ACCCAGCACT 1260
TCTTACATGC TGCGCTCTGA GAGCTTTCCC TCCCCAGTGC CATTCATCCT TGCAACACTC 1320
TCACAGGACA GGCGCTGATA CAATCTGCAT TCTAGAGATG TGGGAACTGG CACAGAGAGG 1380
ACATGACATC AGCCCAAGGT CACAGAGAAA GATGAGCAGA GCCAGAGTTA ACCCCAGCTG 1440
GCTTCCAGAA CCTGTGTTCT AATCCCTCTG GTGCAACCGT CTCCCACACA GAGCTGGTTT 1500
GGATCCCGCC TGCCCTACAT GTTAGCTGCA TGACCCAGGA CATGCTCTTT GGCTTCTCTG 1560
CCTAACCCTC AGTTTCTTTT CTTTTCTTTC TTTTGAGATG GAGTCTCTGT CGCCCAGGCT 1620
GGAGTGCAGT GGCGTGATCT TGGCTCACTC CAACCTCTGC TCTGCCCCCT GGGTTCAAGT 1680
GATTCTTCTG CCTCGGCCTC CCGAGTAGCT GGGATTACAG GCACCCGCCA CCATGCCCGG 1740
CTAATTTTTT TCTATTTTTA GTAGAAACGG GGTCTCACCA TGTTGGCCAG GCTGGTTTCA 1800
AACTCCTGAC CTCAAGTGAT CTGCCTGCCT TGGCTTCCCA AAGTGCTAGG ATTATAGGTG 1860
TGAGCCACCA TACCCGGCCC CCTCAGTTGC TAATCTCTGT AAAGCAGGGT GATGAGACTC 1920
ACCGGATGGC ACTGTTGGTG GGGATGAAAT GAGATGGGAG AGATTAGGTG CTTACTCGGT 1980
GAGCTGCTCA TTGTCACTGT CTCCAAAGGG TGTGGAGCTG TCTGGGGCTG ACTCCAGGCA 2040
CAAGGGACCC CTCCCTGGCC TGTGCATTGC TTAGCATTAC CTGAGATGCT CTTCAGTCCA 2100
TCCCTCCTCC CTACCTCCTC CTCTCTCTTC CTTTTTAAAA AAAATACAGT TTGTTGTAGA 2160
AAAATTAGAA AGTACAGAAA ATGATAGACT AAAAGCAACT TTTAATCCTA CCATGATGTG 2220
TTTCTGTCCA GCTTCTTTGC TAGGCATGTA TGCAAGTATG CATGATTGTT TTTATAGAAC 2280
TGTGGTTTAT TGCACATGCT GTTTCGTGGC TCACCTTTTT TTTTTTTTTT TTTTTTTTTT 2340
AAAGCTAATT ACATATCATG AGCATTTCCC CAGGGGAACT TGTATTGTTT TGCAACAACC 2400
CACATGGCTC TCGATACATT TTTGCCAGGG GTGCAGGGCC TCTCCATGTC TGACCAAGCC 2460
CTGGGGCCCC TGAGATGTCA GGGAGGGAGG TGCATTGCCA CAGAGCAGGA GGCCAGAGGC 2520
TGGGCTTTGG CCCAGCATGT GTGTGGGGGG CCACCTGTAC AGAGATGGCT CCCCAGAGGC 2580
CTCGACGCTC ACTCCCTGCT GAGGTCTGTG ATATGATGCC ACCTGAGGGC CGCTCTGAGA 2640
CTTCCCCTGG GGGGCTTCTC ACTGCTCTCT ACTCATCCAG TAAGGGGATC TGTGACCATG 2700
TGTGGGGTGG CACAGGAGAG ACACACGGGG TCCTGGAAGC CCTCTGTGCA CAGGATGGGC 2760
GGCCACAGAG GGAAGAGGGA ACACATGCAG GTGAGGCCCC 2800
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