EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS149-00653 
Organism
Homo sapiens 
Tissue/cell
NKC 
Coordinate
chr19:45958380-45960630 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSL2MA0478.1chr19:45959150-45959161CTGAGTCACCC-6.02
JUNBMA0490.1chr19:45959150-45959161CTGAGTCACCC-6.02
MYCMA0147.3chr19:45959266-45959278GGGCACGTGGCC-7.22
Number of super-enhancer constituents: 39             
IDCoordinateTissue/cell
SE_01498chr19:45958813-45960047Adrenal_Gland
SE_02108chr19:45958499-45960183Aorta
SE_02406chr19:45958430-45960350Astrocytes
SE_03036chr19:45958768-45959960Bladder
SE_06640chr19:45958730-45960254Brain_Hippocampus_Middle
SE_09930chr19:45956713-45960693CD14
SE_11261chr19:45958545-45960135CD20
SE_13038chr19:45958977-45959634CD34_Primary_RO01480
SE_14395chr19:45958713-45960104CD4_Memory_Primary_7pool
SE_19219chr19:45958648-45960125CD4p_CD25-_Il17p_PMAstim_Th17
SE_20014chr19:45958474-45960238CD56
SE_20748chr19:45959094-45960173CD8_Memory_7pool
SE_22333chr19:45958933-45959876CD8_primiary
SE_23143chr19:45958333-45960000Colon_Crypt_1
SE_23745chr19:45958435-45960006Colon_Crypt_2
SE_24769chr19:45958330-45960073Colon_Crypt_3
SE_26771chr19:45958314-45960076Esophagus
SE_29756chr19:45958492-45960156Fetal_Muscle
SE_31887chr19:45958242-45959952Gastric
SE_34472chr19:45958815-45960056HCT-116
SE_35967chr19:45958253-45960308HMEC
SE_38090chr19:45957862-45960688HUVEC
SE_39922chr19:45958724-45960027K562
SE_41239chr19:45958731-45960085Left_Ventricle
SE_44217chr19:45958500-45960314NHDF-Ad
SE_44830chr19:45958669-45960328NHLF
SE_45809chr19:45956766-45960850Osteoblasts
SE_47661chr19:45958424-45958684Pancreas
SE_47661chr19:45958698-45959895Pancreas
SE_48343chr19:45958657-45960059Psoas_Muscle
SE_49047chr19:45958609-45960056Right_Atrium
SE_50737chr19:45958444-45960123Sigmoid_Colon
SE_51420chr19:45958482-45960430Skeletal_Muscle
SE_52836chr19:45958420-45960076Small_Intestine
SE_53558chr19:45958651-45960115Spleen
SE_57973chr19:45958776-45959093VACO_9m
SE_57973chr19:45959154-45959797VACO_9m
SE_64393chr19:45958339-45960189NHEK
SE_65504chr19:45958083-45960176Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194595942045959846
Number: 1             
IDChromosomeStartEnd
GH19I045453chr194595637045960535
Enhancer Sequence
ACGATCTCGG CTCACTGCAA CCTCCGCCTC CCGGGTTCAA GCGATTCTCC TGCCTCAGGC 60
TCCCAAGTGG CTGGGATAAC AGGTGCCCAC CACTACGCCC AGCTAATTTT TTTTTTTTTT 120
TTAGATAGGG TCTGGCTCTG GCTCTGTCAT ACAGGCTGGA GCACAGTGGC ATGATGACAA 180
CCCACTGCAG CCTTGACCTC CTGGGCTTAA GTGATCCTCT TGCCTCAGCC TCCTGAGTAG 240
CTGGGGCTAC AGGCTTATTT TTTTGTAGAG ATGGGGTCTC ACTCTGTTGC CCAGGCTGGT 300
CTCAAACTTC TGGGCTCAAG CAATCCTCCT GCCTTGGCTT CCCAAAGTGC TGGGTTTACA 360
GGAGTGAGCC ACCATGTCTG GCCATTTGAG GAAATTTTTA TTTTTGTCTG TCTTGTTTCC 420
TGCTCTGTCC CCAGCACCTA GAGTGTGTGA CTGCAGTGTG TGTGTGTGTG TGTGTGTGTG 480
TGTGTGTGTG TGTGTAGGTG TGCTGATTAA ATATTTGAAT GGCTGATTGA ATGAACGAAT 540
GAATGTCATC CTACAACCAC TTGTGAGTCC TGGTCTTAGG GGAAGGCTGG GCTGGGGCCC 600
TGGCCTCTGG GATCCCTCTT GTGCCAGTCC CCCAGCCCTG CTGTTCCCAC AGCTCTGTGC 660
TGAAGAGGGC GTGGAGGGGG CCAGGGAAGG GAGTGTCAGG CAGCCAGCCG GCTGCCTGCC 720
CTGGACAGCA GCCCAGAGTG TCTGCAGGAG GGAGAGGGTA GTTCAGGAGC CTGAGTCACC 780
CTGGGAGAAA CCCCAGCCAC ATACCTGGCC GCTGACATCA CCCGGCCAGG GCACCCCCGG 840
CAGCCTAGAC AAGCTGACTG AATCACAGGC GGAATTCAGC CACCCCGGGC ACGTGGCCTG 900
CTGTGACCCC CCGCAACACC CCCGAGTGGC CGTCTGGCTG CGGGGGTTGG GCCGGGCACA 960
CAGGGGTCAG TGAGGGGGCA TGGGGCCTGA GTCAGGGACA GGGTGGCTAC AGCCAGAGAC 1020
CACCCAGCCA CAGGCGTCCA TGTGGGGCAG GAAGGAGAAA GTTTGGGAAG GAGAGCCTGT 1080
GGGGAGGCCC TGGCGGGTGA GGAGGAAGCA CGTGTGGGTG TGACGGGGAG GCTGCGGCTT 1140
GTGGGCAGCG GCTGGGCGAC CCACAGGGGT GGGATGGGGT CTGAGTGTTT GCGCAGAGAA 1200
TCACCAAATC GTAAGAGACT TGGTCGTAAG AGTCAGTCAG GAGGACAATG GAATCACCAA 1260
TGTGCTTACA CACGCAAAGG CACACACGCA CACTCAACAC CCGGCCTGGG GAGGCCCTGA 1320
CTCCACCCAC CCCAGGCCAG CGGGGCCTCA CTACCCATAA GCCTGCAAGT TCCCTAAGGG 1380
ACTGAGGCCT AAGGGACAGT TTCCTCATCT GTTGAGTGGG GGTATTAACA AGCATTATTA 1440
GGCCAGGCAC AGTGACTCGT GAGGCAGAGG TAGGCGGATC CCTTGGAGGC CAGAAGTTCA 1500
AGACCAGCCT GGACATCATA GCAAGACCCC TTCTCTACAA AGAAAAAATT TAAAAATTAG 1560
CTGGATGTGG TGGTGTGCAC CTGTAGTCCC AGGTACTCAG GAGGCTGTGG AGGGTGGATT 1620
GCTGGAGTGT TGGAGTTTGA GACTGCAGTG AGCTATTGAT TGCACCACTG TACTCCAGCC 1680
TAGACAACAG AACAAGATCC TATAGCAAAA AAAAAAAAAA AAAAAAATCA CTATTATTGT 1740
AATAGCTATG CTTACGGGGA ACATACTTTC TGCCAGGTGC TGTTCTAGGC ATTCTACATT 1800
TTTTTTTTTT AAATAATGGA GATGACGTCT CACTATGTTT CCCAGGCTGG TCTTGAACTC 1860
CTGAGCTCAG GCTATCCTCT CGCTTTTTTG GTGGCTGGCA CGCCTGTAAT CCCGACATTT 1920
TGGGAGGCCA AGGTGGGTGG ATCGCCGGAG CCCAAGAGTT CGAGACCAGC CTGGGAAACA 1980
TAGTGAGATG CCATCTCTAC CAAAAAATCA AAAAATTAGC TAAGCATGGT GGCTCATGCC 2040
TGTAGTCCCA GCTACTCAGG ATGCTGAGGT GGGAGGATCA CTTGAACCTG GGAGATGGAA 2100
GTTGCAGTAA GCTGAGATTG TGCCACTGCA CTCCAGCCTG GGTGACAGAA TAAGACCTTG 2160
TCTCAAAAAA AAAAAAAAAA AAAAAAAAAG AAGAAGAAAA AAGAGAGTCA ACTGCATCTG 2220
TATTTGTGGC ACTTGGTACA TACACGGTAA 2250