EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS191-27856 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr4:10095530-10096840 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2278121chr410096134hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELK1MA0028.2chr4:10095573-10095583CACTTCCGGT-6.02
ELK4MA0076.2chr4:10095572-10095583GCACTTCCGGT+6.02
ERGMA0474.2chr4:10095573-10095583CACTTCCGGT-6.02
ETS1MA0098.3chr4:10095573-10095583CACTTCCGGT-6.02
FEVMA0156.2chr4:10095573-10095583CACTTCCGGT-6.02
FLI1MA0475.2chr4:10095573-10095583CACTTCCGGT-6.02
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_01734chr4:10091052-10105841Aorta
SE_02758chr4:10093747-10100786Astrocytes
SE_04459chr4:10093617-10105385Brain_Anterior_Caudate
SE_05471chr4:10094965-10100815Brain_Cingulate_Gyrus
SE_08364chr4:10093665-10100812Brain_Inferior_Temporal_Lobe
SE_09623chr4:10091018-10105026CD14
SE_12329chr4:10094501-10096206CD3
SE_12329chr4:10096638-10099991CD3
SE_14886chr4:10093993-10103243CD4_Memory_Primary_7pool
SE_17168chr4:10094937-10095837CD4p_CD225int_CD127p_Tmem
SE_17601chr4:10090784-10114776CD4p_CD25-_CD45RAp_Naive
SE_18041chr4:10091010-10113966CD4p_CD25-_CD45ROp_Memory
SE_18604chr4:10090926-10121361CD4p_CD25-_Il17-_PMAstim_Th
SE_19188chr4:10093472-10113740CD4p_CD25-_Il17p_PMAstim_Th17
SE_22779chr4:10093720-10112946CD8_primiary
SE_23672chr4:10094284-10096149Colon_Crypt_1
SE_24384chr4:10094365-10095806Colon_Crypt_2
SE_26123chr4:10094261-10099717Duodenum_Smooth_Muscle
SE_27018chr4:10093509-10096893Esophagus
SE_30028chr4:10092826-10099607Fetal_Muscle
SE_32010chr4:10093988-10096570Gastric
SE_37776chr4:10093270-10101196HSMMtube
SE_38833chr4:10093677-10100765HUVEC
SE_39084chr4:10093529-10099686IMR90
SE_41136chr4:10092955-10100158Left_Ventricle
SE_42597chr4:10093130-10099624Lung
SE_45147chr4:10094081-10096815NHLF
SE_48189chr4:10091204-10100769Psoas_Muscle
SE_48835chr4:10091704-10099911Right_Atrium
SE_50444chr4:10094263-10099771Sigmoid_Colon
SE_51167chr4:10091069-10111939Skeletal_Muscle
SE_52707chr4:10094275-10099639Small_Intestine
SE_55072chr4:10094176-10096631Stomach_Smooth_Muscle
SE_55289chr4:10094971-10096604Thymus
SE_66345chr4:10095514-10096430Jurkat
SE_66345chr4:10096545-10099342Jurkat
SE_69074chr4:10092970-10096960H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr41009617410096294
Number: 1             
IDChromosomeStartEnd
GH04I010091chr41009329910113947
Enhancer Sequence
GCCTGTTTTG AGCTCAAATT TTCCTTATCT ATCAGGAAGG CAGCACTTCC GGTAACAGCC 60
ACAGCTGAGG TTTCCAGCCC TGCTTGGCTC CAGCCTCAAG TGGGAGAACT ATGTGAGGTA 120
TGAGGTCCCC GCAGGGCAGA GGCAATGGAA CAGAGGGAGC AGTGGCACCC CAGTGAGGGA 180
AGCCAGAAGT CTTCCGTGCT GAACATTTTT CCACCTACAA TCACAGCTTG TTAGATCTGG 240
CAGTGAGTTC TCAGTTCTGC ATCATAAGGC TGAGCCCCCA GGACGACATG CTGCTCTAAG 300
TAACCATTTC ATTAGACACA AACTATCCAG TGCACCACCA ACTCCTGGGA CCTAGGACAT 360
GCACACAGCT GTGAGCCACA CTCCAGAGGG GGCGTGTGGT CATCCTAGAC CACCAAACCA 420
ACTGCTCACC CGACCGGAGG AAGCGGATGG CCAGAGAGGC AAAGAACCTG GCCCAAGTAA 480
TGCGCATGGC GAAGGCAGAC AACAGAGAGA AACTCAGTGG GGCCTTTAAA CCCATCCAGG 540
AGTACCTATC CCAGGAGCCT GCCTGGCATG AAGACATCCC CATGGGTGAG ATGGGGGAAG 600
GCAGGGAGAT GGTCTCGCCA CCCTCCCTTT TTCAGGCCAC GGTCAGACCC TCTGAGGGGA 660
ACCTACCCCT GGGTTCGCAA AATGCCAGTG CTGGAGACCC GAGACCACGG TGCCCAGGGT 720
CTCCTTTCAG AACCGTTCTC CTGTAACCCC GGAAGTTACT TCCGCAGGTC ACCTACCGCG 780
TCTTCAATGT CACTGGGTAG GAATGAGCCG GCACCCAGGC TTATTCCAGG CCAAATGTTC 840
CTCCACTCCC ATCTTCCTGG AGCCTCATTC AGGCAAATGA AGACCAAAGC TGGGCTACGG 900
TCCCTCAGGA CGAGGGGCAC ACAGGGAATG CTGCTTGCAT TTCAGCTCAG GCACAGCATC 960
ATGGAGTTCT GCTTCAGCTT GTACTGAAAC GCCTTCAGAA CATGCCTTGT TCCTTTTCAA 1020
GGCAGCAGCT CCAACACGAC CCAGCTGGTC CCTCCGCAGT CATACGCCAG TCCCTCTCCC 1080
ACCTGGGTAA CTAGGGAAGC ACCTGCCACC CCAGCGCTGC ACCCCCAAGC TCAGGGCAGC 1140
TTCCTGGTCC CGGCCACAGG GGGCCTCTGC AGGGAGTGGG TGCAGAAGGC GCAGATGAAG 1200
ACAGGCCCGA GTTGCCACCA CAGCTGCTCA TTCTCAGGAG GCGAGGGGCG GCAGGCAAGG 1260
CCACCAAGGC CTGAGCGCTG GTGCGGAGGC AAAGGCAGCC CAGACTCAGC 1310