EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS191-11900 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr14:65190390-65192280 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr14:65192090-65192110GGGATGGTGGTGGTGGGTGG-6.68
RREB1MA0073.1chr14:65192097-65192117TGGTGGTGGGTGGGTGGGGT-8.17
SOX10MA0442.2chr14:65191704-65191715TGCTTTGTTTT-6.02
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_03251chr14:65190497-65192006Brain_Angular_Gyrus
SE_03953chr14:65190319-65195292Brain_Anterior_Caudate
SE_04856chr14:65180505-65197762Brain_Cingulate_Gyrus
SE_05821chr14:65180438-65199821Brain_Hippocampus_Middle
SE_06781chr14:65180403-65192060Brain_Hippocampus_Middle_150
SE_06781chr14:65192065-65195493Brain_Hippocampus_Middle_150
SE_07938chr14:65190169-65194504Brain_Inferior_Temporal_Lobe
SE_08852chr14:65191093-65191347Brain_Mid_Frontal_Lobe
SE_19856chr14:65188989-65195748CD4p_CD25-_Il17p_PMAstim_Th17
SE_20478chr14:65185982-65194236CD56
SE_22874chr14:65186008-65194196CD8_primiary
SE_23289chr14:65190472-65194123Colon_Crypt_1
SE_24426chr14:65190542-65191692Colon_Crypt_2
SE_24426chr14:65191797-65193408Colon_Crypt_2
SE_26750chr14:65181719-65194103Esophagus
SE_27717chr14:65189231-65195032Fetal_Intestine
SE_28783chr14:65190366-65194949Fetal_Intestine_Large
SE_32308chr14:65191226-65191696Gastric
SE_32308chr14:65191832-65193491Gastric
SE_36148chr14:65181584-65194566HMEC
SE_49272chr14:65190395-65192755Right_Atrium
SE_50477chr14:65190429-65195289Sigmoid_Colon
SE_54434chr14:65186992-65191038Spleen
SE_54434chr14:65191114-65192192Spleen
SE_57093chr14:65190453-65193416VACO_400
SE_57603chr14:65191232-65191706VACO_503
SE_57603chr14:65191845-65193429VACO_503
SE_64475chr14:65185799-65194369NHEK
SE_65298chr14:65181865-65199543Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr146519048565190694
chr146519071665191649
Number: 1             
IDChromosomeStartEnd
GH14I064714chr146518085865194899
Enhancer Sequence
GTATTTTTAG TAGAGATGGG GTTTCACCAT GTTGGCCTGG CCAGTCTCAA ACTCCTGACC 60
TCAAGTGATC TGCCCCCCTC TGCCTCCCAC AGTGCTGGGA TTACAGGCGT GAGCCATCAT 120
GCCTGGCCGA GAAAGCGAGT TTTCTAGAAG ACTGATTCAC TGATTGATGA CTGACTGGAT 180
TGATTCATGT TGCAAGATGG AAGAGGTCAT GGCTGGGGCA TACTTAAGAG AACTGGAGAC 240
CCGTATGTGG TAGGATGGGG TAGGCGTGGG TACCTGGTTT GAGGGTTTGG TTGCTGCCTG 300
CCTCATCACC TCCTTCTCTG GCCTCCTACT TCCCTAGCAG ACAGGGTCTT CCGAGATGTG 360
TTTGAAGACC TGAGTTCTCA TCCTGGCTTG GGGGAATCTT ATAGTATGGA GTGGTGCTCT 420
TCAGGTAGGA AGGAAAGGCT GACCCCGCCC GGGGAGCACC AGGGGAGGCA CTTTAACTGT 480
CTCTGTGGGA GTCTGAGCTA CACACACATA ATGGTTCCAA TCCGGTGTCT TAGGGCCAGA 540
ATGCACTCCA GCTGAGTGCA GTGCACTCAG AATGCACTCT GAGAGCGATG CCTCTTATCC 600
GTCACCATCA AACGGTGCCT CCTGACAGTC TGCACTAGTG TCCTGCTTTG TACTCAGTGC 660
CTCATTTGTT CTTCAGCCCT CCCTTTCTTG GGCTCTTGGC TCTTTTCCAG CAAGTCCTCC 720
TGCCCAAGAG AGAGAGAGCC TTGTGATCGT GGGTCTCCTG GTCACTACAG GGCTTCTCTC 780
GTCATCCAAG AAGTTTATAG TCCAATCCTG GTGACCTCAT ACTTTCTCCC TCTTCCTTTC 840
TGCTTACCCA TGACCTGTGA TCCTTTGACC GGGAATCTGT ATTTTACCAT ATTGTTCCAG 900
CCAGAGAATG AATGGCCAAA GGTCACATAG TAGCAGGCCC AAAAACTGCC CTAAGGAATC 960
TTGACTCAGT CCTTCCGAGT GTCATGTCAT AAGCCCCAAT CCTTCAGGTC TTCATATGTC 1020
CCCTGCAGCT TATGCTGAAG CAAAGCCATG GCAGCCAGGG CTGTGACCAA TCCTTTGCTT 1080
GTGGCCCTGT CTGGTGTGTA GTCCATTAGG GAGGCAGTGG GCAGGAGAGC ATGAACTCTG 1140
GAGCCTCAGT GCCTGAGTTC AAGTCCAGGC TCTACCACTT ACTACTTCTG TGGCCTCAGT 1200
ACCTGCATGT ATAAAATGAG GGTAGTAATA GAACCTACCT TCTGGAGTTG TTGCAAGGGG 1260
TTAGGCACTT TAATATATAC AGAGCGCTCA GAGCATTTCA GCAGTTGGCT GTTATGCTTT 1320
GTTTTAGCCT TAGGAGATAG GAGCTTAGTT TGCAGACAGG TAGCCTATGA TCAATCAGAG 1380
AGAAAACTTC TGTAAGTAGA AAAGACATAT TAGTTTCTGG GTTTGAAGTG TGCTTATGTT 1440
GCTATCCTCT TACAGTGGGA TCCCCAGAGA GGGACCCTCA AAAGGTCCCT TTTAGAGACA 1500
AATCTCCCTA ATGGTGTGTG TGTTGGGGTA GGGGTGGGGC TGTGAGTAAT CTTTTGCTTT 1560
AAGACTGTGA ACTGGCTGGC TGTGAAATCC ATTTGGGAGT GGGGCCGTTT CCATTTAGCT 1620
TCCCCAGAGA AGCTGACTGA CCCCAGATGT GATCTGGGAA AGGTCTTAGG CTGTAAATCC 1680
CTGCCCCTTT GTTCCCTGCT GGGATGGTGG TGGTGGGTGG GTGGGGTGCC TAACTGCAGT 1740
GCACTTTGAA GGACATCAGA GTGCCACAGG GCTGGGGGTT AAGGGCTGGG GTGGAGCTTG 1800
GGTTTTTATC TGTCAGTGCT GGAATGACAT GGTGTTGCCC TGCCTGCTGG TTCTGTAAAA 1860
GGCATAGCTG ATTAATTGTA AAGGCCCTTT 1890