EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS047-27968 
Organism
Homo sapiens 
Tissue/cell
Fetal_placenta 
Coordinate
chr5:172219470-172221840 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr5:172221271-172221282GGTGACTCATT+6.02
Sox3MA0514.1chr5:172221785-172221795AAAACAAAGG-6.02
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_00085chr5:172214644-172229976Adipose_Nuclei
SE_00944chr5:172220541-172221896Adrenal_Gland
SE_01555chr5:172215762-172224185Aorta
SE_02290chr5:172220910-172221875Astrocytes
SE_02948chr5:172221436-172221896Bladder
SE_09165chr5:172220010-172230001CD14
SE_14398chr5:172220610-172222090CD4_Memory_Primary_7pool
SE_25789chr5:172220458-172229277Duodenum_Smooth_Muscle
SE_26519chr5:172220427-172221959Esophagus
SE_29599chr5:172219096-172223439Fetal_Muscle
SE_31376chr5:172220884-172223019Gastric
SE_36923chr5:172218457-172223922HSMMtube
SE_39983chr5:172220341-172221858K562
SE_40610chr5:172220295-172224071Left_Ventricle
SE_44640chr5:172219584-172230323NHDF-Ad
SE_44768chr5:172220789-172224191NHLF
SE_46262chr5:172219586-172230428Osteoblasts
SE_47360chr5:172220829-172221921Panc1
SE_48206chr5:172219471-172223247Psoas_Muscle
SE_48563chr5:172220385-172221919Right_Atrium
SE_50124chr5:172220102-172221917Sigmoid_Colon
SE_51114chr5:172217685-172227437Skeletal_Muscle
SE_52338chr5:172220100-172221910Small_Intestine
SE_53284chr5:172219661-172224097Spleen
SE_54705chr5:172220880-172223664Stomach_Smooth_Muscle
SE_55249chr5:172219620-172220011Thymus
SE_55249chr5:172220034-172221279Thymus
SE_55249chr5:172221435-172221699Thymus
SE_55716chr5:172219260-172230390u87
SE_61533chr5:172191523-172278016Toledo
SE_62363chr5:172184582-172235488Tonsil
SE_65260chr5:172220442-172221712Pancreatic_islets
SE_67508chr5:172219260-172230390u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5172221140172221536
Number: 1             
IDChromosomeStartEnd
GH05I172787chr5172214436172231054
Enhancer Sequence
GCTGGAGTGC AGTGGCAATC CTAGCTCACT CCATCCTTAA ACTTCTCGGC TCAAGCAATC 60
CTCCTGTCTC AGCCTCCCAA GTAGCTGGGA CTACAGGTGT GCACCACCAT GCCTGGCTAA 120
TTTTTTTGGT TTTTTTTTGG TCTTTTGCAC AGACAGGTTC TCACTATGTT GCCCAGGATG 180
ATCCTGGCCT CAAGCAATCC TCCCATCTTG GGCTCCCAAA GTGCTGGGAT TACAGGCATA 240
AGCCATTGCA TCTGGCCTCT GCTGCTACTG CTAATTCCCT CTGGATCTTT CCAGATGACT 300
CCAGTCCGTC TGAAGCCCCT TCATTCCTGC CCTGGGCTGT CACCCAGCAA TTCCTGGGGG 360
TGGGGGCACT GAGGCCCATG AGCGTCCTTA CTCTAAATGG CCCCAGAGTG CTGGGTGAAG 420
TGGGGTCAGC CAAGAGCCCT GGGCAGTGGA GCAGGGCTTC TATCCTGGCT CTGCCTGTGG 480
TTTGTGGCAG CCTCAGGCTG GGCATCTCTC CCCTTGGGGC CTCCACATTC TCGTGGTAAG 540
GTAGCAGATG ATCTAAAATA AGATTGTGAT CTCCACTGCC TCTTTGATGG CACAGACTCC 600
GTTATTCTAT TTTTGCGTCT TCTGTTAGTA GCATCGTTGT CCTCAACAGT AGCGAGCATT 660
TATTGAACAC CTGTTTTATG CCAGAGACTA AACTTGGTGG TTTGTATCAT GGTAGCTATC 720
AGTTACTGCA TGCTCGGATC CACCAGCCAT AAGCGCGTGG CAGGAGCGTC TCATTCAATC 780
ATCACAGATC CCTTCTGGGG AGGAATTATG ATCATCCCAA CCATAAGGAT GAGCAAAGCA 840
GGTTCCACAT GATGAGATGC CCTCATTCTG CCAATTTGGA CGTAATCACC AAACCATGCC 900
CAAATCCCAC TGCTCTGTGA AGGAGGAATT TTCATCTCCC ATTCATTGAT TAAAGAAAAA 960
CCAAAACCCG CTGCCCAGAG AGGGGAAGTG ACTCAGCCCT CATCCCACTG TTTGAGATGG 1020
TGGCCTCTGA GGACATTCTG CCTCTACTCT CTATCTTCTT TGATGCCAAT GGTCTCAGCT 1080
GAGGCTTCAA AGAAATGTGA CCTGGGCTTT GTGACTCCCA GTTCCTCCTC AGAATTCCTG 1140
TTCAGTTACT CTGGGCCTAC AGTGGACTCC AGGTAACTAA GGGTCTAGCC TTTGGCCAGA 1200
GGTCTGACCT CCAGATAAAC TTGAGCTCTA GGGAAGAAAG GCACAGACCA TGGAAGGTCA 1260
CACCGTCTCC ACTGCTCCTT CCTCCCTGAA GCTCAAGCAG GGGCTTCTTC CCACCTGGGC 1320
CACCTGCTCC GTGATGCACC CACGTTATCT TCTTTGTGGC CTGTGACAAT TTCCTGGCTC 1380
GGGATGAGGA GCTTCATTTT GCAGATGAGG AAATTGAGGT CGAATGGTTT ATCCAAGCAG 1440
GGAATCATTC GGTGGTGCCC CAGGCAAATA ATATTATCAA GGACGCTTTT TAAAATTCCA 1500
GCAGACTGGA GAGGGTGGGT TGTTTTTCCA CTTTTGGGTA AGGATTTTGG ACTTCAGCCT 1560
GCAGGCCCTG CCTCCAGCCA GGCAGAGGAA AAGGTCGCAT GAGAGACGCA GCTCTGGTTC 1620
AAAGGTCCCT CACGGAGAAG CCTTTTCCTT CCAGCAGCCG CCACGGAAGG CCGACTTACT 1680
TGCTCTTTTC AGGCCTCTAT TATACTTGCC TTTTACCCCT AAGAGCAAAG AAAAGAGGAA 1740
GCTGCTGTTT GCTTTCTGGA GGCCCAGGCA AAGTGAAAAT AGGAGCACCC ATGAGAAAGA 1800
TGGTGACTCA TTCCCTGACG GAGGGACCAG GCCAGCTAGA GCAGAGGGGC CTTGGGAAGA 1860
CCTGGGCTTT TGTTCCTTTT GGGACCAAAA TGAATCACTG ATCTCATTAA GTCACACCGG 1920
CCAGTCCCGA ACTTTCCCGG GTAGAACCAC TGCAAGCATC AAATCTTAGG TGAGGCCCCA 1980
TCAATGGTCA TGAACAGGAG CAAAAAGGTT GAGCTTCTCC TCATTCAAAA GGCCAGAAAA 2040
GACCTTGTTC TCCTTGGAGC AAAGTGGTAA CTGGACCCAG AAGAGGAAGG TCAGGCACGA 2100
TGCCTCGAAC AAGGCCGGTC AGCAAGGTGG TAGCCCCCTA CCTAGGCACA CTAGTGCTTT 2160
GGGACGCCAT ACAACACACC CACTCATTTG CCCATGGATT CAGACAGGGA GTCAGCAAGC 2220
ATTGACAGGA CATCCAGCTG GTGCCAGGTG TTCTACATGC CATCTCTTCT CCAGACCCTG 2280
CATAAGAGGA AGAGGAGCCT CATTCCACAG ACAAGAAAAC AAAGGTGGCT GGGCGCAGTG 2340
ACTCACCCCT GTAATCCCAG CACTTTGGAA 2370