EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS191-13422 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr15:67369550-67370880 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs12901071chr1567370389hg19
rs12901372chr1567370506hg19
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_02047chr15:67369842-67370778Aorta
SE_09181chr15:67366082-67371152CD14
SE_10181chr15:67366164-67371299CD19_Primary
SE_10875chr15:67354078-67404812CD20
SE_14469chr15:67368065-67370713CD4_Memory_Primary_7pool
SE_17822chr15:67368660-67371356CD4p_CD25-_CD45ROp_Memory
SE_18371chr15:67364370-67371368CD4p_CD25-_Il17-_PMAstim_Th
SE_19163chr15:67368109-67370952CD4p_CD25-_Il17p_PMAstim_Th17
SE_23212chr15:67369614-67371249Colon_Crypt_1
SE_23998chr15:67369744-67370844Colon_Crypt_2
SE_25827chr15:67368302-67371308Duodenum_Smooth_Muscle
SE_26536chr15:67369832-67370882Esophagus
SE_27694chr15:67369393-67371461Fetal_Intestine
SE_28551chr15:67369321-67371497Fetal_Intestine_Large
SE_31411chr15:67369701-67370930Gastric
SE_32497chr15:67368255-67371005GM12878
SE_34355chr15:67368112-67369800HCT-116
SE_34355chr15:67369821-67370682HCT-116
SE_34728chr15:67366732-67370465HeLa
SE_36917chr15:67364416-67376637HSMMtube
SE_37941chr15:67366127-67370517HUVEC
SE_40033chr15:67368138-67370877K562
SE_42172chr15:67369741-67370838Lung
SE_44149chr15:67369632-67370642NHDF-Ad
SE_44749chr15:67368688-67371076NHLF
SE_45534chr15:67364411-67371470Osteoblasts
SE_47100chr15:67357928-67475420Panc1
SE_48052chr15:67366504-67374901Psoas_Muscle
SE_50064chr15:67368620-67371374Sigmoid_Colon
SE_51081chr15:67366276-67376636Skeletal_Muscle
SE_52344chr15:67368168-67371321Small_Intestine
SE_53518chr15:67369913-67370745Spleen
SE_58377chr15:67342858-67447290Ly1
SE_59897chr15:67354926-67408793Ly4
SE_60508chr15:67357006-67428179DHL6
SE_61631chr15:67357404-67427415Toledo
SE_62286chr15:67356723-67443338Tonsil
SE_64236chr15:67369816-67370788NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr156737007667370710
Number: 1             
IDChromosomeStartEnd
GH15I067072chr156736434167371314
Enhancer Sequence
GCATTTCTGT ATGTATGTAT GTATGTACGT ATGTATGTAT GTATGTATTT ATTTTTGTAG 60
CATCCGCTCA GTTGCGTGGC CACAACTGAA TCCCAGTCCA GGTGGCACCA TTATATGGGT 120
AGCATTTTGG AGATGTTCAC AGGAATTGAT TTCCCTCACC CTCAACCCAG GCCAGAGTGA 180
ATTTAATGCA GATGAGGGAG AAGGTGCTAC ATATTATAGC TGCTCATTCA AAAAGTGGAG 240
CAGAGAGCTG GACCACTGAA TGTGCCTTTG TTTGCTGGAA ATCTTTATTA AGTACCAGAG 300
ATATAGAGAT GAAGTTGTGT CTCTGAACTG CTCAGAGGCA AAAAAGGGAC ACCAGTAACC 360
ACAGTTATGG TGGGCCTGTG GAAGAGACAC TATAGTGAAG GTCAAACAAA ATATTTGGGA 420
GCCTAGAGGA AGAACAGGTC TATTTCTGGA GGTATCAGAA GGCTTCACAG AGGAGGCAAT 480
ACTCAATTGG GGCCTTGAAG GATGGATAGG AGTGTAGGAG TGGAGTGGGA GGCAGCACAG 540
AGCACAGACC AGACTGCGGA AGGGCCTGAC ATCTAGGGAA GGCAAGACAG TTTAGGGTGG 600
CCAGAGTGTG GATGAGGGAG TGGCCAGAGA GGAGTTGGAG AAGGATGTTG TCAAGGGCTT 660
TGGCTTGCCA AACTTCGTAC TTTGTGTTTG GACCTTGCTC TGTAAGTGTC CAGGAGATTT 720
TAAAGCAGGG GAGTGGCACG GTGAAAGCCA CCACTCTATC GTTTCTTGTT TCATTTCCTC 780
CTCTTACCCA GTGGCTGTTA ACAGCAGGTT TTCTGCCCGA GTTATCCAGG TCAGAGTCAT 840
AATCCCTTAC AGTACCATGT GGACAGCTTT AGGCTATGTC TGGAGCAGGT TGAAGATAGT 900
GTTTTGTTCA CTGTCAGGAG AGAAGACATG TTGTTCAGCC AGGAGGGCTC AGGGACCCCA 960
GGCGTTCAGG TAATTAGCCA GTGAGTCATG TCAGGCTTTT GATATGGATA CCTTGGGAAA 1020
CTAAGTGGGG TGTTGCTGGC CTCCATGCAG ATGCCTGGTC TACCCAAGCA CAGGCCCCCA 1080
AATTAGATCT CGGCCTCTGC TGGGTCTTCC CTGTGCCTGA CACAGTGCCT TCATATGGAC 1140
CGTCTCTGGT CAGTGTTTTC AATTTCTTTG TTGATGATCA TCAATCAAGG CCAGGCTTTC 1200
CAATTCCAGA CCACACTGCA ATCAGTGGAA ACTACCTAAA TTCAGTACTG CAGACCCATA 1260
GCAGGATGTA TGTTTATTGA AAACAGATTA TATTCCTTAA TGAGAGACTA AAACAGCATG 1320
TTTAAATCAG 1330