EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS146-06798 
Organism
Homo sapiens 
Tissue/cell
NHDF 
Coordinate
chr17:76376230-76378730 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4082919chr1776377482hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOSMA0476.1chr17:76377934-76377945TCTGACTCATT+6.32
IRF1MA0050.2chr17:76376921-76376942TTTTTCTTTTTCTTTTTTTTT+6.09
IRF1MA0050.2chr17:76376915-76376936TTTTTCTTTTTCTTTTTCTTT+6.17
RESTMA0138.2chr17:76378102-76378123GGCAGTACCTTGGAGAGGTCA+6.4
ZNF263MA0528.1chr17:76378308-76378329AGGGGATGGAGGGAGGGAAGA+6.27
ZNF263MA0528.1chr17:76378312-76378333GATGGAGGGAGGGAAGAAGAG+6.58
Number of super-enhancer constituents: 25             
IDCoordinateTissue/cell
SE_00336chr17:76373804-76385436Adipose_Nuclei
SE_02571chr17:76377096-76378499Astrocytes
SE_06227chr17:76376990-76378950Brain_Hippocampus_Middle
SE_09402chr17:76373053-76385593CD14
SE_18476chr17:76373745-76385519CD4p_CD25-_Il17-_PMAstim_Th
SE_19399chr17:76373920-76383558CD4p_CD25-_Il17p_PMAstim_Th17
SE_26825chr17:76377089-76378750Esophagus
SE_29662chr17:76377085-76378700Fetal_Muscle
SE_31461chr17:76377276-76378724Gastric
SE_38195chr17:76373184-76383376HUVEC
SE_40802chr17:76377083-76378729Left_Ventricle
SE_42104chr17:76376113-76376772Lung
SE_42104chr17:76377101-76378838Lung
SE_44143chr17:76376006-76378857NHDF-Ad
SE_44787chr17:76373967-76376972NHLF
SE_44787chr17:76376985-76378790NHLF
SE_45620chr17:76370124-76383364Osteoblasts
SE_48690chr17:76377189-76378837Right_Atrium
SE_50089chr17:76377057-76378804Sigmoid_Colon
SE_51088chr17:76376802-76385058Skeletal_Muscle
SE_52389chr17:76377118-76378821Small_Intestine
SE_53327chr17:76376882-76383569Spleen
SE_55689chr17:76377240-76378461u87
SE_58926chr17:76309354-76389031Ly3
SE_62409chr17:76309367-76385525Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr177637733776378350
chr177637735076378568
Enhancer Sequence
GCCACCGTGC CCGGCTGCAA ATAGGTTTCT TAATTGAGTC TTACACTTGA TCTTTAAAAA 60
AAAAAATCTT AGAACTGCTT CCTTTAGTTG AGGTTGCATT GTGTTAGATT TTCTATCTGT 120
ACGTGTACTC CTCGGGTGAG ATTTGACCTC CTGGGGTCAG ACATCTAGTA CAGAGATCTG 180
GGGTCCAGTC ATGTGTACTG ATTCTAGGTA CAGAAAAGAG CTTGCTTCAT GGTGATCTAT 240
GGTGGAAGAT TTTCATCGAA AACTCAAGTT TGATTTAGGG GAATTTTTAG GTGATAGAAT 300
CAGGGCAGGA TGGCGCTCTT GGAAACCTGC TAGGTTTCAC GTTGGTGAAC CCAGCAGGAC 360
TGGGGCTGTA AAAGAAATGG CCTCTGCATT TTTTGCATTT TCATTTTTTC AGTGTTTAAC 420
AAAAGACCTG CTCATCTCTG GGTGACGAAG TCAGATGACT TCTACGTCCT GGCATCAAAC 480
CACTGAGATT TGGTTTACAG TTTCAAAAAA ATGTTCTACC CTTGAAGACA AGATTTAGGT 540
GACTTTGTCA TTTCCCTCTA TATGTTTAAA CTATATGAAA AACACTTCAT TATAAATCAT 600
TGTTCAACAT TGGAATTGAT TACTAAAGGA TGTTGGGGCA GTTGACACAA ATATTTTAAA 660
AAAGAAATCT CTCATGAGTG TGCTTTTTTT CTTTTTCTTT TTCTTTTTTT TTTTGAGACA 720
GAGTCTTGTT CTGTCACTCA GGCTGGAGTG CAGTGGTCTG ATCTCGGCTC AGTGCAACCT 780
CTACCTCGTG GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC AGAGTAGCTG GGTCTACAGA 840
CACATGCCAC CACGTCCGGC TAATTTTTGT ATCTTTAGTA GAGACAGGGT TTCACCATGT 900
TGGCCAGGCT GGCCTCGATC TCCTGACCTT GTAACCTGCC CACCTCGGCC TCCCACAGTG 960
CTGGGATTAC AGGTGTGAGC CACTGCGCCC AGCCACTTTT TTGTTTTTTG GTGGTGGGAG 1020
GGGCAGTGTG GCAGTGGAGA TAGTCTAAAT TGACTTTCTA ATCTCTTTTT TTTGTAAATT 1080
GTGTGAGTGG ATGCAGTTTG TGTGCCTTCA TCCTTCATTA AGCTGAGAGA GATGATTGTT 1140
TCTCTGGGAC AACAGTTCAA CCAGCAACTC AGTTTCTTGG GCATTAAGAC AGAAGTTTTT 1200
GCTTTGTAAT CCTCGGAAAT AATGCCTATG GTAGGACTGA GGATAAATGC TTTGACCGGT 1260
ATTGAGTGGT AGTGTAGGTT TCTGAGCCTT TCTTTGCCTT ATTCGGTTTG CAGTTCTTTT 1320
CTGATTCGTT GTGGCCTTGG TGTTCGAGTT ATTCATGTTT GTTGTGGCTG CTTACCCTTT 1380
ATTAGCTGCT GACTTTGCTT TCTTCTCCAT TATTCAGTTG CACCTCCCAA TTTCTCATTC 1440
CCCGAATGAT GTGGTTTCTT GTAACTCGCT GATCATTGAT TCATTGATAA TAGTTCTGTG 1500
CAGTCATGAG CTTGAATTAT TTTAGGTTTT AGCTTGTCGA TCTGAGTCAG CTGTTGGAGG 1560
GCCAGTGAAC CCTCGTGAGG GGACGTTCCT TTTACTGCCG CGGTTTCCTT TCAGGCATAG 1620
AGACAGCCAG AGAGACAGAG AACTCTACTT AAAATTACTT CTGTTAATGA TTTAGAAGCA 1680
CTGTCATTTC CTCTTAAGCT AGCATCTGAC TCATTATCAT TAGGAACTGC TGGATCCGTT 1740
AATTTATTCA TCATGTGTGT ATTGAGCACT GCTGTGCTGT GCTAGGTACT CAGGAAGCAA 1800
AGATAAAGAC ACAGCCCCAC CTCCAAGACG CTCAGACCCA TAAACAATTA CAAGAAGTAG 1860
GTAGAAGGTC ATGGCAGTAC CTTGGAGAGG TCATGGAAGG CTTCCTGGTG CAGTGGCTCA 1920
TAGCTGTTTT GAAGGAGGGG TCGGAGTAGT TAGGCTCGGT GAAGAAGAGG GGGAGTGGAT 1980
GTTCAAGAAG TGATAGTGAC ATGGACTGCA GCGAAAGGCA ATTCTGAGGT CCCACCAATA 2040
CTGAAACCAT TTCCAGGAGC TGACTAGGGG TACCGAGTAG GGGATGGAGG GAGGGAAGAA 2100
GAGGAGCTAG GAGCAAGCCA GTCTGGGCCA GAGACCCAGG AAGACAAGTT CTGAGATTCC 2160
ATGTATGATT TCTTTTGATT CTGGTTCAGC CTGAGATGGT GGGGGCTTTT ATATGAAGTC 2220
GGGGCAGTGG GAGCAGAAAA GAGGGCTGAG TGAGAATCAG TCTTGATGGG GCACATGGAT 2280
GTTGGTACAT TTCACGAAAA CGGAGTAAAG AAGAGGCTCA GGTTTTGGGG ATGATGGTAA 2340
AGTGCATTTG GGTTATGTTA ATCAGTATCC AGGTTCCTCT AGGTGATGTG TTCAGTGTCC 2400
AGTTGACTGT GGCAGAACTG GAGCTCAGGA GAGGGAGACA GATGCTTCAG ATAGGGTTTT 2460
TTTGAGTCAT CCGGCTACAC AGAATGGTTT TTTTTTTTTT 2500