| Tag | Content |
|---|
EnhancerAtlas ID | HS073-08317 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr2:70000180-70003060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr2:70001040-70001051 | CATGAGTCACC | - | 6.62 | | Foxd3 | MA0041.1 | chr2:70000688-70000700 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr2:70000692-70000704 | GTTTGTTTGTTT | + | 6.32 | | JUND | MA0491.1 | chr2:70001040-70001051 | CATGAGTCACC | - | 6.02 | | LBX2 | MA0699.1 | chr2:70000554-70000564 | GCCAATTAGC | + | 6.02 | | MEF2A | MA0052.3 | chr2:70001125-70001137 | GCTATTTTTAGT | - | 6.18 | | MEF2B | MA0660.1 | chr2:70001125-70001137 | GCTATTTTTAGT | - | 6.62 | | MEF2C | MA0497.1 | chr2:70001124-70001139 | TGCTATTTTTAGTAG | - | 6.48 | | Nr2f6(var.2) | MA0728.1 | chr2:70000982-70000997 | TGAACTCCTGACCTC | - | 6.22 | | RUNX1 | MA0002.2 | chr2:70001861-70001872 | CTCTGTGGTTT | + | 6.14 | | ZNF263 | MA0528.1 | chr2:70000455-70000476 | TCCCCCTTCCCTGCCTCCTCA | - | 7.26 | | ZNF740 | MA0753.2 | chr2:70001459-70001472 | CCCCCCCCCCCCC | + | 6.03 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_26278 | chr2:69999794-70000939 | Duodenum_Smooth_Muscle | | SE_27649 | chr2:70000042-70000876 | Fetal_Intestine | | SE_27649 | chr2:70001945-70012834 | Fetal_Intestine | | SE_28548 | chr2:69988829-70001642 | Fetal_Intestine_Large | | SE_28548 | chr2:70001663-70014048 | Fetal_Intestine_Large | | SE_31933 | chr2:70000284-70000709 | Gastric | | SE_31933 | chr2:70000966-70001467 | Gastric | | SE_31933 | chr2:70001543-70003068 | Gastric | | SE_37647 | chr2:69999849-70000912 | HSMMtube | | SE_53176 | chr2:70000219-70000835 | Small_Intestine | | SE_53176 | chr2:70002283-70002956 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr2 | 70000275 | 70000707 | | chr2 | 70000495 | 70000634 | | chr2 | 70001639 | 70003000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I069761 | chr2 | 69988613 | 70010508 |
|
Enhancer Sequence | TTTGTACTAG TAAAACTTTA ATAAATAAAC AACAGCTGTC TGTATATAAA TGTGTATATT 60
ACACTGTGTG CTGTCCAAGT TTCAAAATAA ATTGAATAAA AGTACCCAGT GTTCAAGTAT 120
GATACCTTCT TTTTCCTTAA GTGAAATATT TCTAGCTCCT TGTGTAATGA CTCTCAGTAT 180
TTCCAGAAGG CTTTGCTCAA GATGTCTTTC CACTTCTTGA TGTGGTAAAA AGGAGTGGAA 240
TGTTCATATT AAAGCTTGCC TCTTTTGGAG AGGTGTCCCC CTTCCCTGCC TCCTCACTTG 300
TCATTTATTC CAAAACTACA TGAAAGCAAA GGGAAGGCCC TTGCTCTGAA AAGCAGTATC 360
TGCCAGGGTT GTCAGCCAAT TAGCATATGA ATCATACTTA CCAAGGGATA TGGGTACATG 420
TGGATCATTC ACATGACATG AAACAGGGCC TCCAGACCAA GGACTGGCTA AGATCTGTGA 480
AGGTCTTAAG TTTTGCCCCT GATTTTTTGT TTGTTTGTTT GTTTATCAAT ATTTGTTTTA 540
TTCTCCTTTC TTTTCTTTTC TTTTCTTTCC TTCTTTTTTT TTTTTTTTTT TTTTTTTGTT 600
TTCGACAGAG TCTTGCTCTG TCACCCAGGC TAGAGTGCAG TGGCGTGATC TCAGCTCACT 660
GCAACCTCTG CCTCCTGGGT TCAAGCAATT CTACTTCCTC AGCCTCCCGA GTATCTGGGA 720
TTACAGGCGT GCACCACCAC GCCTGGCTAA TTTTTGTATT TTTAGTAGAG ACGGGGTTTC 780
ACCATATTGG TCAGGCTGGT CTTGAACTCC TGACCTCGTG ATTCGCCTGC CTCGGCCTCC 840
CAAAGTGCTG GGATTACAGG CATGAGTCAC CGCGCCCGTC CTCAAGCAAT TCTTGTACCT 900
CAGCCTCCCT AGTAGCTGGG ATTACAGGCA TGCCAGGCTA ATTTTGCTAT TTTTAGTAGA 960
GGCAGGGTTT CACCGTGTTG GCCAGGCTGG TCTCGAACTC CTGACCTCAG GTGATCTGCC 1020
CGCCCCTGCC TCCCACAATG CTGGGATTAC AGGCGTGAGC CATCTCACCC TGCCCTATGT 1080
GTTAATAACC ATTTAAAAAT TTCCACCCTG CTAAGACTAG TCCGTGACTC TCTGTGCCTT 1140
TCTCCATTCT TCTCTTAACT AACCTCATGT TTTTATTAGC ATCTGTAAGA CCCATAAGGG 1200
GAAACTGAGA GAGAAAATTC AATAAGACTC CCTTGGTTTT GCAGCAGTAA GGTTATATGA 1260
GGTGTTTATG TAAAAGGAGC CCCCCCCCCC CCTTTTTTTT TTTTTTTGAG ACAGAGTTTC 1320
GCTCTTGTTG CCCAGGTTGG AGAGCAGTGG CGCAATCTCA GCTCACTGCA ACCTCCGCCT 1380
CCCAGGTTCA AGTGATTCTT CTGCCTCAGC CTTCCGAGTA GCTGGGATTA CAGGCACCCG 1440
CCACCATGCC TGACTAATTG TTTGTATATT TAGTAGAGAC GGGGTTTCAT CAGGTTGGCC 1500
AGGCTGGTCT CAAACTCCTG ACCTCAGGTA GTCCACCCAC CTCGGCCTCC CAAAGTGCAG 1560
AGATTACAGG CGTGAGCCAC CGCGTCCAGC CAAAAGGAGC CCCCTTAATC ACAGCGTTTA 1620
CCATGACCTG GGTAACAGGC ATATTCAGCA GACAAATACC CCGATGATCA TCAAGCCAGT 1680
CCTCTGTGGT TTGCATATGA AGCACATCAG CTGCTTCATC AGGGGTATTC TACTTGGCAT 1740
TTATAAGGGG AGAGGAACAG TCCCCCTTCT CAGGGTAAAC AGACCTTAGT GTGGCTTTTG 1800
TCCAGTCCAC CAGGCTGGAT GTTCTCTCAG GAATAACCTC CTATGTGTCT GGACCACCTG 1860
AAACATCTGC GATTGCTCCA TAGAGAGCTG TGGGTCCTGC ATCAACCCAA ACATGAATGC 1920
TAGCATTTTG AATACTCTGC AGTGTTCGAA ACCTAAGACA CTGTCACTCA CTTAGTTACT 1980
CACACAACCC ATTTGAATAA AGGTTCTTCA GGAAGTTTAT GATACTGATC TACAAAATGA 2040
AATAACTTCT TCACACTATA CCCTGTGGTT TCAATCGTTT CATGGTTTGC CTTCCACCCC 2100
ACATAAACTG CCTTCTTGGT TACCAGAGTT CTTAGTGATA TTGTCTAATC TCAGCATGAT 2160
TTTGCCATTG GTGGGTGGCT TTGCAGTTAC TGGCTAGAGC GCAGACTCAC TGAAATCTGA 2220
GCTTGGTCTG ACCCAGCACT CTCTTTTAAT TTTATTTTAT CTGTTACAGA TAATAACCAA 2280
GGGACTGAAT ATATCGCCTT TTCTTATTAG TTTGCATTTC CTTATGCTTC CAGTGAGCCA 2340
ACACCTTGGG GTAGCTTTTA CCTTTACTAA CAGATCTCAG CATGGTATGC TACTCCGTAC 2400
CATGAGTGGC TGTTACCAAT GCCATGGGTT CTTGTAATCA CCCAGGATAG AAATCAAGAG 2460
CAATCACCAT ACATAGCAGC AAAGAGAAAG TTTGTTTTGG CTCATGCACA AGGGAGCCAG 2520
TGCTGAGAAA GGAAAAGAAA CAGACTGCTA TCGGAGGATA GTGTGTGGGT TAGTTTTATA 2580
GGGTCTTTCC ATGGGAAAGG GTTACATCAG AGCATGTATA GGAGAGGCTT TTCTAGCACT 2640
CATGCTTCTT CATGCATCAT ATGCAACATT AGTATTTTAA ATCTCCACCC CATGCATTTT 2700
TAGCCTTAAA ATGAGGAAGG GTAACTGTAG GTTGGACTTT AAGTCTAGCT ATGCATGCAG 2760
GGCTCCAGGG AAGTCCCCAG CCCCCTGAAA TAGGAACTCG TGGTTAATAA GCTTCTTGGG 2820
TCTTTTGTTA TTAATTGGCT GAGAGTTAGA TAAGTTAAAG CTTGAGTGAA TGGCTTCTAT 2880
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